Maize Event DP-004114-3 and Methods for Detection Thereof

ABSTRACT

The invention provides DNA compositions that relate to transgenic insect resistant maize plants. Also provided are assays for detecting the presence of the maize DP-004114-3 event based on the DNA sequence of the recombinant construct inserted into the maize genome and the DNA sequences flanking the insertion site. Kits and conditions useful in conducting the assays are provided.

CROSS REFERENCE

This utility application claims the benefit U.S. Provisional ApplicationNo. 61/617,990 filed Mar. 30, 2012, which is incorporated herein byreference in its entirety.

REFERENCE TO SEQUENCE LISTING SUBMITTED ELECTRONICALLY

The official copy of the sequence listing is submitted electronicallyvia EFS-Web as an ASCII formatted sequence listing with a file named“5251_sequence_listing.txt” created on Mar. 8, 2013, and having a sizeof 51 kilobytes and is filed concurrently with the specification. Thesequence listing contained in this ASCII formatted document is part ofthe specification and is herein incorporated by reference in itsentirety.

FIELD OF INVENTION

Embodiments of the present invention relate to the field of plantmolecular biology, specifically embodiment of the invention relate toDNA constructs for conferring insect resistance to a plant. Embodimentsof the invention more specifically relate to insect resistant corn plantevent DP-004114-3 and to assays for detecting the presence of corn eventDP-004114-3 in a sample and compositions thereof.

BACKGROUND OF INVENTION

An embodiment of this invention relates to the insect resistant corn(Zea mays) plant DP-004114-3, also referred to as “maize lineDP-004114-3,” “maize event DP-004114-3,” and “4114 maize,” and to theDNA plant expression construct of corn plant DP-004114-3 and thedetection of the transgene/flanking insertion region in corn plantDP-004114-3 and progeny thereof.

Corn is an important crop and is a primary food source in many areas ofthe world. Damage caused by insect pests is a major factor in the lossof the world's corn crops, despite the use of protective measures suchas chemical pesticides. In view of this, insect resistance has beengenetically engineered into crops such as corn in order to controlinsect damage and to reduce the need for traditional chemicalpesticides. One group of genes which have been utilized for theproduction of transgenic insect resistant crops is the delta-endotoxingroup from Bacillus thuringiensis (Bt). Delta-endotoxins have beensuccessfully expressed in crop plants such as cotton, potatoes, rice,sunflower, as well as corn, and have proven to provide excellent controlover insect pests. (Perlak, F. J et al. (1990) Bio/Technology 8:939-943;Perlak, F. J. et al. (1993) Plant Mol. Biol. 22:313-321; Fujimoto, H. etal. (1993) Bio/Technology 11:1151-1155; Tu et al. (2000) NatureBiotechnology 18:1101-1104; PCT publication WO 01/13731; and Bing, J. W.et al. (2000) Efficacy of Cry1F Transgenic Maize, 14^(th) BiennialInternational Plant Resistance to Insects Workshop, Fort Collins,Colo.).

The expression of foreign genes in plants is known to be influenced bytheir location in the plant genome, perhaps due to chromatin structure(e.g., heterochromatin) or the proximity of transcriptional regulatoryelements (e.g., enhancers) close to the integration site (Weising et al.(1988) Ann. Rev. Genet. 22:421-477). At the same time the presence ofthe transgene at different locations in the genome will influence theoverall phenotype of the plant in different ways. For this reason, it isoften necessary to screen a large number of events in order to identifyan event characterized by optimal expression of an introduced gene ofinterest. For example, it has been observed in plants and in otherorganisms that there may be a wide variation in levels of expression ofan introduced gene among events. There may also be differences inspatial or temporal patterns of expression, for example, differences inthe relative expression of a transgene in various plant tissues, thatmay not correspond to the patterns expected from transcriptionalregulatory elements present in the introduced gene construct. For thisreason, it is common to produce hundreds to thousands of differentevents and screen those events for a single event that has desiredtransgene expression levels and patterns for commercial purposes. Anevent that has desired levels or patterns of transgene expression isuseful for introgressing the transgene into other genetic backgrounds bysexual outcrossing using conventional breeding methods. Progeny of suchcrosses maintain the transgene expression characteristics of theoriginal transformant. This strategy is used to ensure reliable geneexpression in a number of varieties that are well adapted to localgrowing conditions.

It would be advantageous to be able to detect the presence of aparticular event in order to determine whether progeny of a sexual crosscontain a transgene of interest. In addition, a method for detecting aparticular event would be helpful for complying with regulationsrequiring the pre-market approval and labeling of foods derived fromrecombinant crop plants, for example, or for use in environmentalmonitoring, monitoring traits in crops in the field, or monitoringproducts derived from a crop harvest, as well as for use in ensuringcompliance of parties subject to regulatory or contractual terms.

It is possible to detect the presence of a transgene by any nucleic aciddetection method known in the art including, but not limited to, thepolymerase chain reaction (PCR) or DNA hybridization using nucleic acidprobes. These detection methods generally focus on frequently usedgenetic elements, such as promoters, terminators, marker genes, etc.,because for many DNA constructs, the coding region is interchangeable.As a result, such methods may not be useful for discriminating betweendifferent events, particularly those produced using the same DNAconstruct or very similar constructs unless the DNA sequence of theflanking DNA adjacent to the inserted heterologous DNA is known. Forexample, an event-specific PCR assay is described in U.S. Pat. No.6,395,485 for the detection of elite event GAT-ZM1. Accordingly, itwould be desirable to have a simple and discriminative method for theidentification of event DP-004114-3.

SUMMARY OF INVENTION

Embodiments of this invention relate to methods for producing andselecting an insect resistant monocot crop plant. More specifically, aDNA construct is provided that when expressed in plant cells and plantsconfers resistance to insects. According to one aspect of the invention,a DNA construct, capable of introduction into and replication in a hostcell, is provided that when expressed in plant cells and plants confersinsect resistance to the plant cells and plants. Maize event DP-004114-3was produced by Agrobacterium-mediated transformation with plasmidPHP27118. This event contains the cry1F, cry34Ab1, cry35Ab1, and patgene cassettes, which confer resistance to certain lepidopteran andcoleopteran pests, as well as tolerance to phosphinothricin.

Specifically, the first cassette contains a truncated version of thecry1F gene from Bacillus thuringiensis var. aizawai. The insertion ofthe cry1F gene confers resistance to damage by lepidopteran pests. TheCry1F protein (SEQ ID NO: 1) is comprised of 605 amino acids and has amolecular weight of approximately 68 kDa. The expression of the cry1Fgene is controlled by the maize polyubiquitin promoter (Christensen etal. (1992) Plant Mol. Biol. 118(4):675-89), providing constitutiveexpression of the Cry1F protein in maize. This region also includes the5′ untranslated region (UTR) and intron associated with the nativepolyubiquitin promoter. The terminator for the cry1F gene is the poly(A)addition signal from Open Reading Frame 25 (ORF 25) of the Agrobacteriumtumefaciens Ti plasmid pTi15955 (Barker et al. (1983) Plant Mol. Biol.2:335-350).

The second cassette contains the cry34Ab1 gene isolated from Bacillusthuringiensis strain PS149B1 (U.S. Pat. Nos. 6,127,180; 6,624,145 and6,340,593). The Cry34Ab1 protein (SEQ ID NO: 2) is 123 amino acidresidues in length and has a molecular weight of approximately 14 kDa.The expression of the cry34Ab1 gene is controlled by a second copy ofthe maize polyubiquitin promoter with 5′ UTR and intron (Christensen etal., 1992, supra). The terminator for the cry34Ab1 gene is the pinIIterminator (Keil et al. (1986) Nucleic Acids Res. 14:5641-5650; An etal. (1989) Plant Cell 1:115-22).

The third gene cassette contains the cry35Ab1 gene, also isolated fromBacillus thuringiensis strain PS149B1 (U.S. Pat. Nos. 6,083,499;6,548,291 and 6,340,593). The Cry35Ab1 protein (SEQ ID NO: 3) has alength of 383 amino acids and a molecular weight of approximately 44kDa. Simultaneous expression of the Cry34Ab1 and Cry35Ab1 proteins inthe plant confers resistance to coleopteran insects. The expression ofthe cry35Ab1 gene is controlled by the Triticum aestivum (wheat)peroxidase promoter and leader sequence (Hertig et al. (1991) Plant Mol.Biol. 16:171-174). The terminator for the cry35Ab1 gene is a second copyof the pinII terminator (Keil et al., 1986, supra; An et al., 1989,supra).

The fourth and final gene cassette contains a version of thephosphinothricin acetyl transferase gene from Streptomycesviridochromogenes (pat) that has been optimized for expression in maize.The pat gene expresses the phosphinothricin acetyl transferase enzyme(PAT) that confers tolerance to phosphinothricin. The PAT protein (SEQID NO: 4) is 183 amino acids residues in length and has a molecularweight of approximately 21 kDa. Expression of the pat gene is controlledby the promoter and terminator regions from the CaMV 35S transcript(Franck et al. (1980) Cell 21:285-294; Odell et al. (1985) Nature313:810-812; Pietrzak, et al. (1986) Nucleic Acids Res.14(14):5857-5868). Plants containing the DNA constructs are alsoprovided.

According to another embodiment of the invention, compositions andmethods are provided for identifying a novel corn plant designatedDP-004114-3. The methods are based on primers or probes whichspecifically recognize the 5′ and/or 3′ flanking sequence ofDP-004114-3. DNA molecules are provided that comprise primer sequencesthat when utilized in a PCR reaction will produce amplicons unique tothe transgenic event DP-004114-3. The corn plant and seed comprisingthese molecules is an embodiment of this invention. Further, kitsutilizing these primer sequences for the identification of theDP-004114-3 event are provided.

An additional embodiment of the invention relates to the specificflanking sequence of DP-004114-3 described herein, which can be used todevelop specific identification methods for DP-004114-3 in biologicalsamples. More particularly, the invention relates to the 5′ and/or 3′flanking regions of DP-004114-3 which can be used for the development ofspecific primers and probes. A further embodiment of the inventionrelates to identification methods for the presence of DP-004114-3 inbiological samples based on the use of such specific primers or probes.

According to another embodiment of the invention, methods of detectingthe presence of DNA corresponding to the corn event DP-004114-3 in asample are provided. Such methods comprise: (a) contacting the samplecomprising DNA with a DNA primer set, that when used in a nucleic acidamplification reaction with genomic DNA extracted from corn eventDP-004114-3 produces an amplicon that is diagnostic for corn eventDP-004114-3; (b) performing a nucleic acid amplification reaction,thereby producing the amplicon; and (c) detecting the amplicon.

According to another embodiment of the invention, methods of detectingthe presence of a DNA molecule corresponding to the DP-004114-3 event ina sample, such methods comprising: (a) contacting the sample comprisingDNA extracted from a corn plant with a DNA probe molecule thathybridizes under stringent hybridization conditions with DNA extractedfrom corn event DP-004114-3 and does not hybridize under the stringenthybridization conditions with a control corn plant DNA; (b) subjectingthe sample and probe to stringent hybridization conditions; and (c)detecting hybridization of the probe to the DNA. More specifically, amethod for detecting the presence of a DNA molecule corresponding to theDP-004114-3 event in a sample, such methods, consisting of (a)contacting the sample comprising DNA extracted from a corn plant with aDNA probe molecule that consists of sequences that are unique to theevent, e.g. junction sequences, wherein said DNA probe moleculehybridizes under stringent hybridization conditions with DNA extractedfrom corn event DP-004114-3 and does not hybridize under the stringenthybridization conditions with a control corn plant DNA; (b) subjectingthe sample and probe to stringent hybridization conditions; and (c)detecting hybridization of the probe to the DNA.

In addition, a kit and methods for identifying event DP-004114-3 in abiological sample which detects a DP-004114-3 specific region areprovided.

DNA molecules are provided that comprise at least one junction sequenceof DP-004114-3; wherein a junction sequence spans the junction betweenheterologous DNA inserted into the genome and the DNA from the corn cellflanking the insertion site, i.e. flanking DNA, and is diagnostic forthe DP-004114-3 event.

According to another embodiment of the invention, methods of producingan insect resistant corn plant that comprise the steps of: (a) sexuallycrossing a first parental corn line comprising the expression cassettesof the invention, which confers resistance to insects, and a secondparental corn line that lacks insect resistance, thereby producing aplurality of progeny plants; and (b) selecting a progeny plant that isinsect resistant. Such methods may optionally comprise the further stepof back-crossing the progeny plant to the second parental corn line toproducing a true-breeding corn plant that is insect resistant.

A further embodiment of the invention provides a method of producing acorn plant that is resistant to insects comprising transforming a corncell with the DNA construct PHP27118, growing the transformed corn cellinto a corn plant, selecting the corn plant that shows resistance toinsects, and further growing the corn plant into a fertile corn plant.The fertile corn plant can be self pollinated or crossed with compatiblecorn varieties to produce insect resistant progeny.

Another embodiment of the invention further relates to a DNA detectionkit for identifying maize event DP-004114-3 in biological samples. Thekit comprises a first primer which specifically recognizes the 5′ or 3′flanking region of DP-004114-3, and a second primer which specificallyrecognizes a sequence within the foreign DNA of DP-004114-3, or withinthe flanking DNA, for use in a PCR identification protocol. A furtherembodiment of the invention relates to a kit for identifying eventDP-004114-3 in biological samples, which kit comprises a specific probehaving a sequence which corresponds or is complementary to, a sequencehaving between 80% and 100% sequence identity with a specific region ofevent DP-004114-3. The sequence of the probe corresponds to a specificregion comprising part of the 5′ or 3′ flanking region of eventDP-004114-3.

The methods and kits encompassed by the embodiments of the presentinvention can be used for different purposes such as, but not limited tothe following: to identify event DP-004114-3 in plants, plant materialor in products such as, but not limited to, food or feed products (freshor processed) comprising, or derived from plant material; additionallyor alternatively, the methods and kits can be used to identifytransgenic plant material for purposes of segregation between transgenicand non-transgenic material; additionally or alternatively, the methodsand kits can be used to determine the quality of plant materialcomprising maize event DP-004114-3. The kits may also contain thereagents and materials necessary for the performance of the detectionmethod.

A further embodiment of this invention relates to the DP-004114-3 cornplant or its parts, including, but not limited to, pollen, ovules,vegetative cells, the nuclei of pollen cells, and the nuclei of eggcells of the corn plant DP-004114-3 and the progeny derived thereof. Thecorn plant and seed of DP-004114-3 from which the DNA primer moleculesprovide a specific amplicon product is an embodiment of the invention.

The foregoing and other aspects of the invention will become moreapparent from the following detailed description and accompanyingdrawing.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Schematic diagram of plasmid PHP27118 with genetic elementsindicated and Hind III restriction enzyme sites. Plasmid size is 54910bp.

FIG. 2. Schematic diagram of the T-DNA indicating the cry1F, cry34Ab1,cry35Ab1, and pat genes (arrows) along with their respective regulatoryelements. Hind III restriction enzyme sites within the T-DNA areindicated. The size of the T-DNA is 11978 bp.

FIG. 3. Schematic Diagram of the Transformation and Development ofDP-004114-3.

FIG. 4. Western corn rootworm (WCRW) larvae developmental effects in thesub-lethal seedling assay employing maize hybrid seedlings in the samegenetic background: DP-004114-3 maize with an isoline as a negativecontrol. Results are based on three replicates. Graphic profiles showthe percent of larvae in each of three instars at 17 days post egghatch. A shift towards instar 3 indicates a decrease in efficacy.

FIG. 5. Schematic representation of the insert and genomic borderregions sequenced in 4114 maize. The diagram indicates the PCR fragmentsgenerated from 4114 maize genomic DNA that were cloned and sequenced:fragments A through F. The vertical dash line represents the genomicborder/insert junctions. Fragment G and H represent the 5′ and 3′genomic border regions, respectively. Figure is not drawn to scale.

DETAILED DESCRIPTION

The following definitions and methods are provided to better define thepresent invention and to guide those of ordinary skill in the art in thepractice of the present invention. Unless otherwise noted, terms are tobe understood according to conventional usage by those of ordinary skillin the relevant art. Definitions of common terms in molecular biologymay also be found in Rieger et al., Glossary of Genetics: Classical andMolecular, 5^(th) edition, Springer-Verlag; New York, 1991; and Lewin,Genes V, Oxford University Press: New York, 1994. The nomenclature forDNA bases as set forth at 37 CFR §1.822 is used.

The following table sets forth abbreviations used throughout thisdocument, and in particular in the Examples section.

TABLE OF ABBREVIATIONS 4114 maize Maize containing event DP-004114-3 bpBase pair Bt Bacillus thuringiensis CaMV Cauliflower mosaic virus cry1Fcry1F gene from Bacillus thuringiensis var. aizawai Cry1F Protein fromcry1F gene cry34Ab1 cry34Ab1 gene from Bacillus thuringiensis strainPS149B1 Cry34Ab1 Protein from cry34Ab1 cry35Ab1 cry35Ab1 gene fromBacillus thuringiensis strain PS149B1 Cry35Ab1 Protein from cry35Ab1gene kb Kilobase pair kDa KiloDalton LB Left T-DNA border patphosphinothricin acetyl transferase gene PAT Protein fromphosphinothricin acetyl transferase gene PCR Polymerase chain reactionpinII Proteinase inhibitor II gene from Solanum tuberosum RB Right T-DNAborder T-DNA The transfer DNA portion of the Agrobacteriumtransformation plasmid between the Left and Right Borders that isexpected to be transferred to the plant genome UTR Untranslated regionECB European corn borer (Ostrinia nubilalis) FAW Fall armyworm(Spodoptera frugiperda) WCRW western corn rootworm (Diabrotica virgiferavirgifera)

Compositions of this disclosure include seed deposited as Patent DepositNo. PTA-11506 and plants, plant cells, and seed derived therefrom.Applicant(s) have made a deposit of at least 2500 seeds of maize eventDP-004114-3 with the American Type Culture Collection (ATCC), Manassas,Va. 20110-2209 USA, on Nov. 24, 2010 and the deposits were assigned ATCCDeposit No. PTA-11506. These deposits will be maintained under the termsof the Budapest Treaty on the International Recognition of the Depositof Microorganisms for the Purposes of Patent Procedure. These depositswere made merely as a convenience for those of skill in the art and arenot an admission that a deposit is required under 35 U.S.C. §112. Theseeds deposited with the ATCC on Nov. 24, 2010 were taken from thedeposit maintained by Pioneer Hi-Bred International, Inc., 7250 NW62^(nd) Avenue, Johnston, Iowa 50131-1000. Access to this deposit willbe available during the pendency of the application to the Commissionerof Patents and Trademarks and persons determined by the Commissioner tobe entitled thereto upon request. Upon allowance of any claims in theapplication, the Applicant(s) will make available to the public,pursuant to 37 C.F.R. §1.808, sample(s) of the deposit of at least 2500seeds of hybrid maize with the American Type Culture Collection (ATCC),10801 University Boulevard, Manassas, Va. 20110-2209. This deposit ofseed of maize event DP-004114-3 will be maintained in the ATCCdepository, which is a public depository, for a period of 30 years, or 5years after the most recent request, or for the enforceable life of thepatent, whichever is longer, and will be replaced if it becomesnonviable during that period. Additionally, Applicant(s) have satisfiedall the requirements of 37 C.F.R. §§1.801-1.809, including providing anindication of the viability of the sample upon deposit. Applicant(s)have no authority to waive any restrictions imposed by law on thetransfer of biological material or its transportation in commerce.Applicant(s) do not waive any infringement of their rights granted underthis patent or rights applicable to event DP-004114-3 under the PlantVariety Protection Act (7 USC 2321 et seq.). Unauthorized seedmultiplication prohibited. The seed may be regulated.

As used herein, the term “comprising” means “including but not limitedto.”

As used herein, the term “corn” means Zea mays or maize and includes allplant varieties that can be bred with corn, including wild maizespecies.

As used herein, the term “DP-004114-3 specific” refers to a nucleotidesequence which is suitable for discriminatively identifying eventDP-004114-3 in plants, plant material, or in products such as, but notlimited to, food or feed products (fresh or processed) comprising, orderived from plant material.

As used herein, the terms “insect resistant” and “impacting insectpests” refers to effecting changes in insect feeding, growth, and/orbehavior at any stage of development, including but not limited to:killing the insect; retarding growth; preventing reproductivecapability; inhibiting feeding; and the like.

As used herein, the terms “pesticidal activity” and “insecticidalactivity” are used synonymously to refer to activity of an organism or asubstance (such as, for example, a protein) that can be measured bynumerous parameters including, but not limited to, pest mortality, pestweight loss, pest attraction, pest repellency, and other behavioral andphysical changes of a pest after feeding on and/or exposure to theorganism or substance for an appropriate length of time. For example“pesticidal proteins” are proteins that display pesticidal activity bythemselves or in combination with other proteins.

“Coding sequence” refers to a nucleotide sequence that codes for aspecific amino acid sequence. As used herein, the terms “encoding” or“encoded” when used in the context of a specified nucleic acid mean thatthe nucleic acid comprises the requisite information to guidetranslation of the nucleotide sequence into a specified protein. Theinformation by which a protein is encoded is specified by the use ofcodons. A nucleic acid encoding a protein may comprise non-translatedsequences (e.g., introns) within translated regions of the nucleic acidor may lack such intervening non-translated sequences (e.g., as incDNA).

“Gene” refers to a nucleic acid fragment that expresses a specificprotein, including regulatory sequences preceding (5′ non-codingsequences) and following (3′ non-coding sequences) the coding sequence.“Native gene” refers to a gene as found in nature with its ownregulatory sequences. “Chimeric gene” refers any gene that is not anative gene, comprising regulatory and coding sequences that are notfound together in nature. Accordingly, a chimeric gene may compriseregulatory sequences and coding sequences that are derived fromdifferent sources, or regulatory sequences and coding sequences derivedfrom the same source, but arranged in a manner different than that foundin nature. “Endogenous gene” refers to a native gene in its naturallocation in the genome of an organism. “Foreign” refers to material notnormally found in the location of interest. Thus “foreign DNA” maycomprise both recombinant DNA as well as newly introduced, rearrangedDNA of the plant. A “foreign” gene refers to a gene not normally foundin the host organism, but that is introduced into the host organism bygene transfer. Foreign genes can comprise native genes inserted into anon-native organism, or chimeric genes. A “transgene” is a gene that hasbeen introduced into the genome by a transformation procedure. The sitein the plant genome where a recombinant DNA has been inserted may bereferred to as the “insertion site” or “target site”.

As used herein, “insert DNA” refers to the heterologous DNA within theexpression cassettes used to transform the plant material while“flanking DNA” can exist of either genomic DNA naturally present in anorganism such as a plant, or foreign (heterologous) DNA introduced viathe transformation process which is extraneous to the original insertDNA molecule, e.g. fragments associated with the transformation event. A“flanking region” or “flanking sequence” as used herein refers to asequence of at least 20 bp, preferably at least 50 bp, and up to 5000bp, which is located either immediately upstream of and contiguous withor immediately downstream of and contiguous with the original foreigninsert DNA molecule. Transformation procedures leading to randomintegration of the foreign DNA will result in transformants containingdifferent flanking regions characteristic and unique for eachtransformant. When recombinant DNA is introduced into a plant throughtraditional crossing, its flanking regions will generally not bechanged. Transformants will also contain unique junctions between apiece of heterologous insert DNA and genomic DNA, or two (2) pieces ofgenomic DNA, or two (2) pieces of heterologous DNA. A “junction” is apoint where two (2) specific DNA fragments join. For example, a junctionexists where insert DNA joins flanking DNA. A junction point also existsin a transformed organism where two (2) DNA fragments join together in amanner that is modified from that found in the native organism.“Junction DNA” refers to DNA that comprises a junction point. Twojunction sequences set forth in this disclosure are the junction pointbetween the maize genomic DNA and the 5′ end of the insert as set forthin SEQ ID NO: 27, and the junction point between the 3′ end of theinsert and maize genomic DNA as set forth in SEQ ID NO: 28.

As used herein, “heterologous” in reference to a nucleic acid is anucleic acid that originates from a foreign species, or, if from thesame species, is substantially modified from its native form incomposition and/or genomic locus by deliberate human intervention. Forexample, a promoter operably linked to a heterologous nucleotidesequence can be from a species different from that from which thenucleotide sequence was derived, or, if from the same species, thepromoter is not naturally found operably linked to the nucleotidesequence. A heterologous protein may originate from a foreign species,or, if from the same species, is substantially modified from itsoriginal form by deliberate human intervention.

“Regulatory sequences” refer to nucleotide sequences located upstream(5′ non-coding sequences), within, or downstream (3′ non-codingsequences) of a coding sequence, and which influence the transcription,RNA processing or stability, or translation of the associated codingsequence. Regulatory sequences may include promoters, translation leadersequences, introns, and polyadenylation recognition sequences.

“Promoter” refers to a nucleotide sequence capable of controlling theexpression of a coding sequence or functional RNA. In general, a codingsequence is located 3′ to a promoter sequence. The promoter sequenceconsists of proximal and more distal upstream elements, the latterelements are often referred to as enhancers. Accordingly, an “enhancer”is a nucleotide sequence that can stimulate promoter activity and may bean innate element of the promoter or a heterologous element inserted toenhance the level or tissue-specificity of a promoter. Promoters may bederived in their entirety from a native gene, or be composed ofdifferent elements derived from different promoters found in nature, oreven comprise synthetic nucleotide segments. It is understood by thoseskilled in the art that different promoters may direct the expression ofa gene in different tissues or cell types, or at different stages ofdevelopment, or in response to different environmental conditions.Promoters that cause a nucleic acid fragment to be expressed in mostcell types at most times are commonly referred to as “constitutivepromoters”. New promoters of various types useful in plant cells areconstantly being discovered; numerous examples may be found in thecompilation by Okamuro and Goldberg (1989) Biochemistry of Plants15:1-82. It is further recognized that since in most cases the exactboundaries of regulatory sequences have not been completely defined,nucleic acid fragments of different lengths may have identical promoteractivity.

The “translation leader sequence” refers to a nucleotide sequencelocated between the promoter sequence of a gene and the coding sequence.The translation leader sequence is present in the fully processed mRNAupstream of the translation start sequence. The translation leadersequence may affect numerous parameters including, processing of theprimary transcript to mRNA, mRNA stability and/or translationefficiency. Examples of translation leader sequences have been described(Turner and Foster (1995) Mol. Biotechnol. 3:225-236).

The “3′ non-coding sequences” refer to nucleotide sequences locateddownstream of a coding sequence and include polyadenylation recognitionsequences and other sequences encoding regulatory signals capable ofaffecting mRNA processing or gene expression. The polyadenylation signalis usually characterized by affecting the addition of polyadenylic acidtracts to the 3′ end of the mRNA precursor. The use of different 3′non-coding sequences is exemplified by Ingelbrecht et al. (1989) PlantCell 1:671-680.

A “protein” or “polypeptide” is a chain of amino acids arranged in aspecific order determined by the coding sequence in a polynucleotideencoding the polypeptide.

A DNA construct is an assembly of DNA molecules linked together thatprovide one or more expression cassettes. The DNA construct may be aplasmid that is enabled for self replication in a bacterial cell andcontains various endonuclease enzyme restriction sites that are usefulfor introducing DNA molecules that provide functional genetic elements,i.e., promoters, introns, leaders, coding sequences, 3′ terminationregions, among others; or a DNA construct may be a linear assembly ofDNA molecules, such as an expression cassette. The expression cassettecontained within a DNA construct comprises the necessary geneticelements to provide transcription of a messenger RNA. The expressioncassette can be designed to express in prokaryote cells or eukaryoticcells. Expression cassettes of the embodiments of the present inventionare designed to express in plant cells.

The DNA molecules of embodiments of the invention are provided inexpression cassettes for expression in an organism of interest. Thecassette will include 5′ and 3′ regulatory sequences operably linked toa coding sequence. “Operably linked” means that the nucleic acidsequences being linked are contiguous and, where necessary to join twoprotein coding regions, contiguous and in the same reading frame.Operably linked is intended to indicate a functional linkage between apromoter and a second sequence, wherein the promoter sequence initiatesand mediates transcription of the DNA sequence corresponding to thesecond sequence. The cassette may additionally contain at least oneadditional gene to be co-transformed into the organism. Alternatively,the additional gene(s) can be provided on multiple expression cassettesor multiple DNA constructs.

The expression cassette will include in the 5′ to 3′ direction oftranscription: a transcriptional and translational initiation region, acoding region, and a transcriptional and translational terminationregion functional in the organism serving as a host. The transcriptionalinitiation region (i.e., the promoter) may be native or analogous, orforeign or heterologous to the host organism. Additionally, the promotermay be the natural sequence or alternatively a synthetic sequence. Theexpression cassettes may additionally contain 5′ leader sequences in theexpression cassette construct. Such leader sequences can act to enhancetranslation.

It is to be understood that as used herein the term “transgenic”includes any cell, cell line, callus, tissue, plant part, or plant, thegenotype of which has been altered by the presence of a heterologousnucleic acid including those transgenics initially so altered as well asthose created by sexual crosses or asexual propagation from the initialtransgenic. The term “transgenic” as used herein does not encompass thealteration of the genome (chromosomal or extra-chromosomal) byconventional plant breeding methods or by naturally occurring eventssuch as random cross-fertilization, non-recombinant viral infection,non-recombinant bacterial transformation, non-recombinant transposition,or spontaneous mutation.

A transgenic “event” is produced by transformation of plant cells with aheterologous DNA construct(s), including a nucleic acid expressioncassette that comprises a transgene of interest, the regeneration of apopulation of plants resulting from the insertion of the transgene intothe genome of the plant, and selection of a particular plantcharacterized by insertion into a particular genome location. An eventis characterized phenotypically by the expression of the transgene. Atthe genetic level, an event is part of the genetic makeup of a plant.The term “event” also refers to progeny produced by a sexual outcrossbetween the transformant and another variety that include theheterologous DNA. Even after repeated back-crossing to a recurrentparent, the inserted DNA and flanking DNA from the transformed parent ispresent in the progeny of the cross at the same chromosomal location.The term “event” also refers to DNA from the original transformantcomprising the inserted DNA and flanking sequence immediately adjacentto the inserted DNA that would be expected to be transferred to aprogeny that receives inserted DNA including the transgene of interestas the result of a sexual cross of one parental line that includes theinserted DNA (e.g., the original transformant and progeny resulting fromselfing) and a parental line that does not contain the inserted DNA.

An insect resistant DP-004114-3 corn plant can be bred by first sexuallycrossing a first parental corn plant consisting of a corn plant grownfrom the transgenic DP-004114-3 corn plant and progeny thereof derivedfrom transformation with the expression cassettes of the embodiments ofthe present invention that confers insect resistance, and a secondparental corn plant that lacks insect resistance, thereby producing aplurality of first progeny plants; and then selecting a first progenyplant that is resistant to insects; and selfing the first progeny plant,thereby producing a plurality of second progeny plants; and thenselecting from the second progeny plants an insect resistant plant.These steps can further include the back-crossing of the first insectresistant progeny plant or the second insect resistant progeny plant tothe second parental corn plant or a third parental corn plant, therebyproducing a corn plant that is resistant to insects.

As used herein, the term “plant” includes reference to whole plants,plant organs (e.g., leaves, stems, roots, etc.), seeds, plant cells, andprogeny of same. Parts of transgenic plants understood to be within thescope of the invention comprise, for example, plant cells, protoplasts,tissues, callus, embryos as well as flowers, stems, fruits, leaves, androots originating in transgenic plants or their progeny previouslytransformed with a DNA molecule of the invention and thereforeconsisting at least in part of transgenic cells, are also an embodimentof the present invention.

As used herein, the term “plant cell” includes, without limitation,seeds, suspension cultures, embryos, meristematic regions, callustissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, andmicrospores. The class of plants that can be used in the methods of theinvention is generally as broad as the class of higher plants amenableto transformation techniques, including both monocotyledonous anddicotyledonous plants.

“Transformation” refers to the transfer of a nucleic acid fragment intothe genome of a host organism, resulting in genetically stableinheritance. Host organisms containing the transformed nucleic acidfragments are referred to as “transgenic” organisms. Examples of methodsof plant transformation include Agrobacterium-mediated transformation(De Blaere et al. (1987) Meth. Enzymol. 143:277) andparticle-accelerated or “gene gun” transformation technology (Klein etal. (1987) Nature (London) 327:70-73; U.S. Pat. No. 4,945,050,incorporated herein by reference). Additional transformation methods aredisclosed below.

Thus, isolated polynucleotides of the invention can be incorporated intorecombinant constructs, typically DNA constructs, which are capable ofintroduction into and replication in a host cell. Such a construct canbe a vector that includes a replication system and sequences that arecapable of transcription and translation of a polypeptide-encodingsequence in a given host cell. A number of vectors suitable for stabletransfection of plant cells or for the establishment of transgenicplants have been described in, e.g., Pouwels et al., (1985; Supp. 1987)Cloning Vectors: A Laboratory Manual, Weissbach and Weissbach (1989)Methods for Plant Molecular Biology, (Academic Press, New York); andFlevin et al., (1990) Plant Molecular Biology Manual, (Kluwer AcademicPublishers). Typically, plant expression vectors include, for example,one or more cloned plant genes under the transcriptional control of 5′and 3′ regulatory sequences and a dominant selectable marker. Such plantexpression vectors also can contain a promoter regulatory region (e.g.,a regulatory region controlling inducible or constitutive,environmentally- or developmentally-regulated, or cell- ortissue-specific expression), a transcription initiation start site, aribosome binding site, an RNA processing signal, a transcriptiontermination site, and/or a polyadenylation signal.

It is also to be understood that two different transgenic plants canalso be mated to produce offspring that contain two independentlysegregating added, exogenous genes. Selfing of appropriate progeny canproduce plants that are homozygous for both added, exogenous genes.Back-crossing to a parental plant and out-crossing with a non-transgenicplant are also contemplated, as is vegetative propagation. Descriptionsof other breeding methods that are commonly used for different traitsand crops can be found in one of several references, e.g., Fehr, inBreeding Methods for Cultivar Development, Wilcos J. ed., AmericanSociety of Agronomy, Madison Wis. (1987).

A “probe” is an isolated nucleic acid to which is attached aconventional detectable label or reporter molecule, e.g., a radioactiveisotope, ligand, chemiluminescent agent, or enzyme. Such a probe iscomplementary to a strand of a target nucleic acid, in the case of thepresent invention, to a strand of isolated DNA from corn eventDP-004114-3 whether from a corn plant or from a sample that includes DNAfrom the event. Probes according to the present invention include notonly deoxyribonucleic or ribonucleic acids but also polyamides and otherprobe materials that bind specifically to a target DNA sequence and canbe used to detect the presence of that target DNA sequence.

“Primers” are isolated nucleic acids that are annealed to acomplementary target DNA strand by nucleic acid hybridization to form ahybrid between the primer and the target DNA strand, then extended alongthe target DNA strand by a polymerase, e.g., a DNA polymerase. Primerpairs of the invention refer to their use for amplification of a targetnucleic acid sequence, e.g., by PCR or other conventional nucleic-acidamplification methods. “PCR” or “polymerase chain reaction” is atechnique used for the amplification of specific DNA segments (see, U.S.Pat. Nos. 4,683,195 and 4,800,159; herein incorporated by reference).

Probes and primers are of sufficient nucleotide length to bind to thetarget DNA sequence specifically in the hybridization conditions orreaction conditions determined by the operator. This length may be ofany length that is of sufficient length to be useful in a detectionmethod of choice. Generally, 11 nucleotides or more in length, 18nucleotides or more, and 22 nucleotides or more, are used. Such probesand primers hybridize specifically to a target sequence under highstringency hybridization conditions. Probes and primers according toembodiments of the present invention may have complete DNA sequencesimilarity of contiguous nucleotides with the target sequence, althoughprobes differing from the target DNA sequence and that retain theability to hybridize to target DNA sequences may be designed byconventional methods. Probes can be used as primers, but are generallydesigned to bind to the target DNA or RNA and are not used in anamplification process.

Specific primers can be used to amplify an integration fragment toproduce an amplicon that can be used as a “specific probe” foridentifying event DP-004114-3 in biological samples. When the probe ishybridized with the nucleic acids of a biological sample underconditions which allow for the binding of the probe to the sample, thisbinding can be detected and thus allow for an indication of the presenceof event DP-004114-3 in the biological sample. Such identification of abound probe has been described in the art. In an embodiment of theinvention the specific probe is a sequence which, under optimizedconditions, hybridizes specifically to a region within the 5′ or 3′flanking region of the event and also comprises a part of the foreignDNA contiguous therewith. The specific probe may comprise a sequence ofat least 80%, between 80 and 85%, between 85 and 90%, between 90 and95%, and between 95 and 100% identical (or complementary) to a specificregion of the event.

Methods for preparing and using probes and primers are described, forexample, in Sambrook et al., Molecular Cloning: A Laboratory Manual,2^(nd) ed., vol. 1-3, Cold Spring Harbor Laboratory Press, Cold SpringHarbor, N.Y. 1989 (hereinafter, “Sambrook et al., 1989”); Ausubel et al.eds., Current Protocols in Molecular Biology, Greene Publishing andWiley-Interscience, New York, 1995 (with periodic updates) (hereinafter,“Ausubel et al., 1995”); and Innis et al., PCR Protocols: A Guide toMethods and Applications, Academic Press: San Diego, 1990. PCR primerpairs can be derived from a known sequence, for example, by usingcomputer programs intended for that purpose such as the PCR primeranalysis tool in Vector NTI version 6 (Informax Inc., Bethesda Md.);PrimerSelect (DNASTAR Inc., Madison, Wis.); and Primer (Version 0.5©,1991, Whitehead Institute for Biomedical Research, Cambridge, Mass.).Additionally, the sequence can be visually scanned and primers manuallyidentified using guidelines known to one of skill in the art.

A “kit” as used herein refers to a set of reagents for the purpose ofperforming the method embodiments of the invention, more particularly,the identification of event DP-004114-3 in biological samples. The kitof the invention can be used, and its components can be specificallyadjusted, for purposes of quality control (e.g. purity of seed lots),detection of event DP-004114-3 in plant material, or material comprisingor derived from plant material, such as but not limited to food or feedproducts. “Plant material” as used herein refers to material which isobtained or derived from a plant.

Primers and probes based on the flanking DNA and insert sequencesdisclosed herein can be used to confirm (and, if necessary, to correct)the disclosed sequences by conventional methods, e.g., by re-cloning andsequencing such sequences. The nucleic acid probes and primers of thepresent invention hybridize under stringent conditions to a target DNAsequence. Any conventional nucleic acid hybridization or amplificationmethod can be used to identify the presence of DNA from a transgenicevent in a sample. Nucleic acid molecules or fragments thereof arecapable of specifically hybridizing to other nucleic acid moleculesunder certain circumstances. As used herein, two nucleic acid moleculesare said to be capable of specifically hybridizing to one another if thetwo molecules are capable of forming an anti-parallel, double-strandednucleic acid structure.

A nucleic acid molecule is said to be the “complement” of anothernucleic acid molecule if they exhibit complete complementarity. As usedherein, molecules are said to exhibit “complete complementarity” whenevery nucleotide of one of the molecules is complementary to anucleotide of the other. Two molecules are said to be “minimallycomplementary” if they can hybridize to one another with sufficientstability to permit them to remain annealed to one another under atleast conventional “low-stringency” conditions. Similarly, the moleculesare said to be “complementary” if they can hybridize to one another withsufficient stability to permit them to remain annealed to one anotherunder conventional “high-stringency” conditions. Conventional stringencyconditions are described by Sambrook et al., 1989, and by Haymes et al.,In: Nucleic Acid Hybridization, a Practical Approach, IRL Press,Washington, D.C. (1985), departures from complete complementarity aretherefore permissible, as long as such departures do not completelypreclude the capacity of the molecules to form a double-strandedstructure. In order for a nucleic acid molecule to serve as a primer orprobe it need only be sufficiently complementary in sequence to be ableto form a stable double-stranded structure under the particular solventand salt concentrations employed.

In hybridization reactions, specificity is typically the function ofpost-hybridization washes, the critical factors being the ionic strengthand temperature of the final wash solution. The thermal melting point(T_(m)) is the temperature (under defined ionic strength and pH) atwhich 50% of a complementary target sequence hybridizes to a perfectlymatched probe. For DNA-DNA hybrids, the T_(m) can be approximated fromthe equation of Meinkoth and Wahl (1984) Anal. Biochem. 138:267-284:T_(m)=81.5° C.+16.6 (log M)+0.41 (% GC)−0.61 (% form)−500/L; where M isthe molarity of monovalent cations, % GC is the percentage of guanosineand cytosine nucleotides in the DNA, % form is the percentage offormamide in the hybridization solution, and L is the length of thehybrid in base pairs. T_(m) is reduced by about 1° C. for each 1% ofmismatching; thus, T_(m), hybridization, and/or wash conditions can beadjusted to hybridize to sequences of the desired identity. For example,if sequences with >90% identity are sought, the T_(m) can be decreased10° C. Generally, stringent conditions are selected to be about 5° C.lower than the T_(m) for the specific sequence and its complement at adefined ionic strength and pH. However, severely stringent conditionscan utilize a hybridization and/or wash at 1, 2, 3, or 4° C. lower thanthe T_(m); moderately stringent conditions can utilize a hybridizationand/or wash at 6, 7, 8, 9, or 10° C. lower than the T_(m); lowstringency conditions can utilize a hybridization and/or wash at 11, 12,13, 14, 15, or 20° C. lower than the T_(m).

Using the equation, hybridization and wash compositions, and desiredT_(m), those of ordinary skill will understand that variations in thestringency of hybridization and/or wash solutions are inherentlydescribed. If the desired degree of mismatching results in a T_(m) ofless than 45° C. (aqueous solution) or 32° C. (formamide solution), itis preferred to increase the SSC concentration so that a highertemperature can be used. An extensive guide to the hybridization ofnucleic acids is found in Tijssen (1993) Laboratory Techniques inBiochemistry and Molecular Biology—Hybridization with Nucleic AcidProbes, Part I, Chapter 2 (Elsevier, New York); and Ausubel et al., eds.(1995) and Sambrook et al. (1989).

As used herein, a substantially homologous sequence is a nucleic acidmolecule that will specifically hybridize to the complement of thenucleic acid molecule to which it is being compared under highstringency conditions. Appropriate stringency conditions which promoteDNA hybridization, for example, 6× sodium chloride/sodium citrate (SSC)at about 45° C., followed by a wash of 2×SSC at 50° C., are known tothose skilled in the art or can be found in Ausubel et al. (1995),6.3.1-6.3.6. Typically, stringent conditions will be those in which thesalt concentration is less than about 1.5 M Na ion, typically about 0.01to 1.0 M Na ion concentration (or other salts) at pH 7.0 to 8.3 and thetemperature is at least about 30° C. for short probes (e.g., 10 to 50nucleotides) and at least about 60° C. for long probes (e.g., greaterthan 50 nucleotides). Stringent conditions may also be achieved with theaddition of a destabilizing agent such as formamide. Exemplary lowstringency conditions include hybridization with a buffer solution of 30to 35% formamide, 1 M NaCl, 1% SDS (sodium dodecyl sulphate) at 37° C.,and a wash in 1× to 2×SSC (20×SSC=3.0 M NaCl/0.3 M trisodium citrate) at50 to 55° C. Exemplary moderate stringency conditions includehybridization in 40 to 45% formamide, 1 M NaCl, 1% SDS at 37° C., and awash in 0.5× to 1×SSC at 55 to 60° C. Exemplary high stringencyconditions include hybridization in 50% formamide, 1 M NaCl, 1% SDS at37° C., and a wash in 0.1×SSC at 60 to 65° C. A nucleic acid of theinvention may specifically hybridize to one or more of the nucleic acidmolecules unique to the DP-004114-3 event or complements thereof orfragments of either under moderately stringent conditions.

Methods of alignment of sequences for comparison are well known in theart. Thus, the determination of percent identity between any twosequences can be accomplished using a mathematical algorithm.Non-limiting examples of such mathematical algorithms are the algorithmof Myers and Miller (1988) CABIOS 4:11-17; the local homology algorithmof Smith et al. (1981) Adv. Appl. Math. 2:482; the homology alignmentalgorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443-453; thesearch-for-similarity-method of Pearson and Lipman (1988) Proc. Natl.Acad. Sci. 85:2444-2448; the algorithm of Karlin and Altschul (1990)Proc. Natl. Acad. Sci. USA 87:2264, modified as in Karlin and Altschul(1993) Proc. Natl. Acad. Sci. USA 90:5873-5877.

Computer implementations of these mathematical algorithms can beutilized for comparison of sequences to determine sequence identity.Such implementations include, but are not limited to: CLUSTAL in thePC/Gene program (available from Intelligenetics, Mountain View, Calif.);the ALIGN program (Version 2.0); the ALIGN PLUS program (version 3.0,copyright 1997); and GAP, BESTFIT, BLAST, FASTA, and TFASTA in theWisconsin Genetics Software Package, Version 10 (available fromAccelrys, 9685 Scranton Road, San Diego, Calif. 92121, USA). Alignmentsusing these programs can be performed using the default parameters.

The CLUSTAL program is well described by Higgins and Sharp, Gene 73:237-244 (1988); Higgins and Sharp, CABIOS 5: 151-153 (1989); Corpet, etal., Nucleic Acids Research 16: 10881-90 (1988); Huang, et al., ComputerApplications in the Biosciences 8: 155-65 (1992), and Pearson, et al.,Methods in Molecular Biology 24: 307-331 (1994). The ALIGN and the ALIGNPLUS programs are based on the algorithm of Myers and Miller (1988)supra. The BLAST programs of Altschul et al. (1990) J. Mol. Biol.215:403 are based on the algorithm of Karlin and Altschul (1990) supra.The BLAST family of programs which can be used for database similaritysearches includes: BLASTN for nucleotide query sequences againstnucleotide database sequences; BLASTX for nucleotide query sequencesagainst protein database sequences; BLASTP for protein query sequencesagainst protein database sequences; TBLASTN for protein query sequencesagainst nucleotide database sequences; and TBLASTX for nucleotide querysequences against nucleotide database sequences. See, Ausubel, et al.,(1995). Alignment may also be performed manually by visual inspection.

To obtain gapped alignments for comparison purposes, Gapped BLAST (inBLAST 2.0) can be utilized as described in Altschul et al. (1997)Nucleic Acids Res. 25:3389. Alternatively, PSI-BLAST (in BLAST 2.0) canbe used to perform an iterated search that detects distant relationshipsbetween molecules. See Altschul et al. (1997) supra. When utilizingBLAST, Gapped BLAST, PSI-BLAST, the default parameters of the respectiveprograms (e.g., BLASTN for nucleotide sequences, BLASTX for proteins)can be used.

As used herein, “sequence identity” or “identity” in the context of twonucleic acid or polypeptide sequences makes reference to the residues inthe two sequences that are the same when aligned for maximumcorrespondence over a specified comparison window. When percentage ofsequence identity is used in reference to proteins it is recognized thatresidue positions which are not identical often differ by conservativeamino acid substitutions, where amino acid residues are substituted forother amino acid residues with similar chemical properties (e.g., chargeor hydrophobicity) and therefore do not change the functional propertiesof the molecule. When sequences differ in conservative substitutions,the percent sequence identity may be adjusted upwards to correct for theconservative nature of the substitution. Sequences that differ by suchconservative substitutions are said to have “sequence similarity” or“similarity.” Means for making this adjustment are well known to thoseof skill in the art. Typically this involves scoring a conservativesubstitution as a partial rather than a full mismatch, therebyincreasing the percentage sequence identity. Thus, for example, where anidentical amino acid is given a score of 1 and a non-conservativesubstitution is given a score of zero, a conservative substitution isgiven a score between zero and 1. The scoring of conservativesubstitutions is calculated, e.g., as implemented in the program PC/GENE(Intelligenetics, Mountain View, Calif.).

As used herein, “percentage of sequence identity” means the valuedetermined by comparing two optimally aligned sequences over acomparison window, wherein the portion of the polynucleotide sequence inthe comparison window may comprise additions or deletions (i.e., gaps)as compared to the reference sequence (which does not comprise additionsor deletions) for optimal alignment of the two sequences. The percentageis calculated by determining the number of positions at which theidentical nucleic acid base or amino acid residue occurs in bothsequences to yield the number of matched positions, dividing the numberof matched positions by the total number of positions in the window ofcomparison, and multiplying the result by 100 to yield the percentage ofsequence identity.

Regarding the amplification of a target nucleic acid sequence (e.g., byPCR) using a particular amplification primer pair, “stringentconditions” are conditions that permit the primer pair to hybridize onlyto the target nucleic-acid sequence to which a primer having thecorresponding wild-type sequence (or its complement) would bind andpreferably to produce a unique amplification product, the amplicon, in aDNA thermal amplification reaction.

The term “specific for (a target sequence)” indicates that a probe orprimer hybridizes under stringent hybridization conditions only to thetarget sequence in a sample comprising the target sequence.

As used herein, “amplified DNA” or “amplicon” refers to the product ofnucleic acid amplification of a target nucleic acid sequence that ispart of a nucleic acid template. For example, to determine whether acorn plant resulting from a sexual cross contains transgenic eventgenomic DNA from the corn plant of the invention, DNA extracted from thecorn plant tissue sample may be subjected to a nucleic acidamplification method using a DNA primer pair that includes a firstprimer derived from flanking sequence adjacent to the insertion site ofinserted heterologous DNA, and a second primer derived from the insertedheterologous DNA to produce an amplicon that is diagnostic for thepresence of the event DNA. Alternatively, the second primer may bederived from the flanking sequence. The amplicon is of a length and hasa sequence that is also diagnostic for the event. The amplicon may rangein length from the combined length of the primer pairs plus onenucleotide base pair to any length of amplicon producible by a DNAamplification protocol. Alternatively, primer pairs can be derived fromflanking sequence on both sides of the inserted DNA so as to produce anamplicon that includes the entire insert nucleotide sequence of thePHP27118 expression construct as well as the sequence flanking thetransgenic insert. A member of a primer pair derived from the flankingsequence may be located a distance from the inserted DNA sequence, thisdistance can range from one nucleotide base pair up to the limits of theamplification reaction, or about 20,000 bp. The use of the term“amplicon” specifically excludes primer dimers that may be formed in theDNA thermal amplification reaction.

Nucleic acid amplification can be accomplished by any of the variousnucleic acid amplification methods known in the art, including PCR. Avariety of amplification methods are known in the art and are described,inter alia, in U.S. Pat. Nos. 4,683,195 and 4,683,202 and in Innis etal., (1990) supra. PCR amplification methods have been developed toamplify up to 22 Kb of genomic DNA and up to 42 Kb of bacteriophage DNA(Cheng et al., Proc. Natl. Acad. Sci. USA 91:5695-5699, 1994). Thesemethods as well as other methods known in the art of DNA amplificationmay be used in the practice of the embodiments of the present invention.It is understood that a number of parameters in a specific PCR protocolmay need to be adjusted to specific laboratory conditions and may beslightly modified and yet allow for the collection of similar results.These adjustments will be apparent to a person skilled in the art.

The amplicon produced by these methods may be detected by a plurality oftechniques, including, but not limited to, Genetic Bit Analysis(Nikiforov, et al. Nucleic Acid Res. 22:4167-4175, 1994) where a DNAoligonucleotide is designed which overlaps both the adjacent flankingDNA sequence and the inserted DNA sequence. The oligonucleotide isimmobilized in wells of a microwell plate. Following PCR of the regionof interest (using one primer in the inserted sequence and one in theadjacent flanking sequence) a single-stranded PCR product can behybridized to the immobilized oligonucleotide and serve as a templatefor a single base extension reaction using a DNA polymerase and labeledddNTPs specific for the expected next base. Readout may be fluorescentor ELISA-based. A signal indicates presence of the insert/flankingsequence due to successful amplification, hybridization, and single baseextension.

Another detection method is the pyrosequencing technique as described byWinge (2000) Innov. Pharma. Tech. 00:18-24. In this method anoligonucleotide is designed that overlaps the adjacent DNA and insertDNA junction. The oligonucleotide is hybridized to a single-stranded PCRproduct from the region of interest (one primer in the inserted sequenceand one in the flanking sequence) and incubated in the presence of a DNApolymerase, ATP, sulfurylase, luciferase, apyrase, adenosine 5′phosphosulfate and luciferin. dNTPs are added individually and theincorporation results in a light signal which is measured. A lightsignal indicates the presence of the transgene insert/flanking sequencedue to successful amplification, hybridization, and single or multi-baseextension.

Fluorescence polarization as described by Chen et al., (1999) GenomeRes. 9:492-498 is also a method that can be used to detect an ampliconof the invention. Using this method an oligonucleotide is designed whichoverlaps the flanking and inserted DNA junction. The oligonucleotide ishybridized to a single-stranded PCR product from the region of interest(one primer in the inserted DNA and one in the flanking DNA sequence)and incubated in the presence of a DNA polymerase and afluorescent-labeled ddNTP. Single base extension results inincorporation of the ddNTP. Incorporation can be measured as a change inpolarization using a fluorometer. A change in polarization indicates thepresence of the transgene insert/flanking sequence due to successfulamplification, hybridization, and single base extension.

Taqman® (PE Applied Biosystems, Foster City, Calif.) is described as amethod of detecting and quantifying the presence of a DNA sequence andis fully understood in the instructions provided by the manufacturer.Briefly, a FRET oligonucleotide probe is designed which overlaps theflanking and insert DNA junction. The FRET probe and PCR primers (oneprimer in the insert DNA sequence and one in the flanking genomicsequence) are cycled in the presence of a thermostable polymerase anddNTPs. Hybridization of the FRET probe results in cleavage and releaseof the fluorescent moiety away from the quenching moiety on the FRETprobe. A fluorescent signal indicates the presence of theflanking/transgene insert sequence due to successful amplification andhybridization.

Molecular beacons have been described for use in sequence detection asdescribed in Tyangi et al. (1996) Nature Biotech. 14:303-308. Briefly, aFRET oligonucleotide probe is designed that overlaps the flanking andinsert DNA junction. The unique structure of the FRET probe results init containing secondary structure that keeps the fluorescent andquenching moieties in close proximity. The FRET probe and PCR primers(one primer in the insert DNA sequence and one in the flanking sequence)are cycled in the presence of a thermostable polymerase and dNTPs.Following successful PCR amplification, hybridization of the FRET probeto the target sequence results in the removal of the probe secondarystructure and spatial separation of the fluorescent and quenchingmoieties. A fluorescent signal results. A fluorescent signal indicatesthe presence of the flanking/transgene insert sequence due to successfulamplification and hybridization.

A hybridization reaction using a probe specific to a sequence foundwithin the amplicon is yet another method used to detect the ampliconproduced by a PCR reaction.

Maize event DP-004114-3 is effective against insect pests includinginsects selected from the orders Coleoptera, Diptera, Hymenoptera,Lepidoptera, Mallophaga, Homoptera, Hemiptera, Orthoptera, Thysanoptera,Dermaptera, Isoptera, Anoplura, Siphonaptera, Trichoptera, etc.,particularly Coleoptera and Lepidoptera.

Insects of the order Lepidoptera include, but are not limited to,armyworms, cutworms, loopers, and heliothines in the family Noctuidae:Agrotis ipsilon Hufnagel (black cutworm); A. orthogonia Morrison(western cutworm); A. segetum Denis & Schiffermuller (turnip moth); A.subterranea Fabricius (granulate cutworm); Alabama argillacea Hübner(cotton leaf worm); Anticarsia gemmatalis Hubner (velvetbeancaterpillar); Athetis mindara Barnes and McDunnough (rough skinnedcutworm); Earias insulana Boisduval (spiny bollworm); E. vittellaFabricius (spotted bollworm); Egira (Xylomyges) curialis Grote (citruscutworm); Euxoa messoria Harris (darksided cutworm); Helicoverpaarmigera Hubner (American bollworm); H. zea Boddie (corn earworm orcotton bollworm); Heliothis virescens Fabricius (tobacco budworm);Hypena scabra Fabricius (green cloverworm); Hyponeuma taltula Schaus;(Mamestra configurata Walker (bertha armyworm); M. brassicae Linnaeus(cabbage moth); Melanchra picta Harris (zebra caterpillar); Mocislatipes Guenée (small mocis moth); Pseudaletia unipuncta Haworth(armyworm); Pseudoplusia includens Walker (soybean looper); Richiaalbicosta Smith (Western bean cutworm); Spodoptera frugiperda JE Smith(fall armyworm); S. exigua Hübner (beet armyworm); S. litura Fabricius(tobacco cutworm, cluster caterpillar); Trichoplusia ni Hübner (cabbagelooper); borers, casebearers, webworms, coneworms, and skeletonizersfrom the families Pyralidae and Crambidae such as Achroia grisellaFabricius (lesser wax moth); Amyelois transitella Walker (navalorangeworm); Anagasta kuehniella Zeller (Mediterranean flour moth);Cadra cautella Walker (almond moth); Chilo partellus Swinhoe (spottedstalk borer); C. suppressalis Walker (striped stem/rice borer); C.terrenellus Pagenstecher (sugarcane stem borer); Corcyra cephalonicaStainton (rice moth); Crambus caliginosellus Clemens (corn rootwebworm); C. teterrellus Zincken (bluegrass webworm); Cnaphalocrocismedinalis Guenee (rice leaf roller); Desmia funeralis Hübner (grapeleaffolder); Diaphania hyalinata Linnaeus (melon worm); D. nitidalisStoll (pickleworm); Diatraea flavipennella Box; D. grandiosella Dyar(southwestern corn borer), D. saccharalis Fabricius (surgarcane borer);Elasmopalpus lignosellus Zeller (lesser cornstalk borer); Eoreumaloftini Dyar (Mexican rice borer); Ephestia elutella Hübner (tobacco(cacao) moth); Galleria mellonella Linnaeus (greater wax moth);Hedylepta accepta Butler (sugarcane leafroller); Herpetogrammalicarsisalis Walker (sod webworm); Homoeosoma electellum Hulst(sunflower moth); Loxostege sticticalis Linnaeus (beet webworm); Marucatestulalis Geyer (bean pod borer); Orthaga thyrisalis Walker (tea treeweb moth); Ostrinia nubilalis Hübner (European corn borer); Plodiainterpunctella Hübner (Indian meal moth); Scirpophaga incertulas Walker(yellow stem borer); Udea rubigalis Guenée (celery leaftier); andleafrollers, budworms, seed worms, and fruit worms in the familyTortricidae Acleris gloverana Walsingham (Western blackheaded budworm);A. variana Fernald (Eastern blackheaded budworm); Adoxophyes oranaFischer von Rösslerstamm (summer fruit tortrix moth); Archips spp.including A. argyrospila Walker (fruit tree leaf roller) and A. rosanaLinnaeus (European leaf roller); Argyrotaenia spp.; Bonagota salubricolaMeyrick (Brazilian apple leafroller); Choristoneura spp.; Cochylishospes Walsingham (banded sunflower moth); Cydia latiferreana Walsingham(filbertworm); C. pomonella Linnaeus (codling moth); Endopiza viteanaClemens (grape berry moth); Eupoecilia ambiguella Hubner (vine moth);Grapholita molesta Busck (oriental fruit moth); Lobesia botrana Denis &Schiffermüller (European grape vine moth); Platynota flavedana Clemens(variegated leafroller); P. stultana Walsingham (omnivorous leafroller);Spilonota ocellana Denis & Schiffermuller (eyespotted bud moth); andSuleima helianthana Riley (sunflower bud moth).

Selected other agronomic pests in the order Lepidoptera include, but arenot limited to, Alsophila pometaria Harris (fall cankerworm); Anarsialineatella Zeller (peach twig borer); Anisota senatoria J. E. Smith(orange striped oakworm); Antheraea pernyi Guérin-Méneville (Chinese OakSilkmoth); Bombyx mori Linnaeus (Silkworm); Bucculatrix thurberiellaBusck (cotton leaf perforator); Collas eurytheme Boisduval (alfalfacaterpillar); Datana integerrima Grote & Robinson (walnut caterpillar);Dendrolimus sibiricus Tschetwerikov (Siberian silk moth), Ennomossubsignaria Hübner (elm spanworm); Erannis tiliaria Harris (lindenlooper); Erechthias flavistriata Walsingham (sugarcane bud moth);Euproctis chrysorrhoea Linnaeus (browntail moth); Harrisina americanaGuérin-Méneville (grapeleaf skeletonizer); Heliothis subflexa Guenée;Hemileuca oliviae Cockrell (range caterpillar); Hyphantria cunea Drury(fall webworm); Keiferia lycopersicella Walsingham (tomato pinworm);Lambdina fiscellaria fiscellaria Hulst (Eastern hemlock looper); L.fiscellaria lugubrosa Hulst (Western hemlock looper); Leucoma salicisLinnaeus (satin moth); Lymantria dispar Linnaeus (gypsy moth);Malacosoma spp.; Manduca quinquemaculata Haworth (five spotted hawkmoth, tomato hornworm); M. sexta Haworth (tomato hornworm, tobaccohornworm); Operophtera brumata Linnaeus (winter moth); Orgyia spp.;Paleacrita vemata Peck (spring cankerworm); Papilio cresphontes Cramer(giant swallowtail, orange dog); Phryganidia californica Packard(California oakworm); Phyllocnistis citrella Stainton (citrusleafminer); Phyllonorycter blancardella Fabricius (spotted tentiformleafminer); Pieris brassicae Linnaeus (large white butterfly); P. rapaeLinnaeus (small white butterfly); P. napi Linnaeus (green veined whitebutterfly); Platyptilia carduidactyla Riley (artichoke plume moth);Plutella xylostella Linnaeus (diamondback moth); Pectinophoragossypiella Saunders (pink bollworm); Pontia protodice Boisduval &Leconte (Southern cabbageworm); Sabulodes aegrotata Guenée (omnivorouslooper); Schizura concinna J. E. Smith (red humped caterpillar);Sitotroga cerealella Olivier (Angoumois grain moth); Telchin licus Drury(giant sugarcane borer); Thaumetopoea pityocampa Schiffermuller (pineprocessionary caterpillar); Tineola bisselliella Hummel (webbingclothesmoth); Tuta absoluta Meyrick (tomato leafminer) and Yponomeutapadella Linnaeus (ermine moth).

Of interest are larvae and adults of the order Coleoptera includingweevils from the families Anthribidae, Bruchidae, and Curculionidaeincluding, but not limited to: Anthonomus grandis Boheman (boll weevil);Cylindrocopturus adspersus LeConte (sunflower stem weevil); Diaprepesabbreviatus Linnaeus (Diaprepes root weevil); Hypera punctata Fabricius(clover leaf weevil); Lissorhoptrus oryzophilus Kuschel (rice waterweevil); Metamasius hemipterus hemipterus Linnaeus (West Indian caneweevil); M. hemipterus sericeus Olivier (silky cane weevil); Sitophilusgranarius Linnaeus (granary weevil); S. oryzae Linnaeus (rice weevil);Smicronyx fulvus LeConte (red sunflower seed weevil); S. sordidusLeConte (gray sunflower seed weevil); Sphenophorus maidis Chittenden(maize billbug); S. livis Vaurie (sugarcane weevil); Rhabdoscelusobscurus Boisduval (New Guinea sugarcane weevil); flea beetles, cucumberbeetles, rootworms, leaf beetles, potato beetles, and leafminers in thefamily Chrysomelidae including, but not limited to: Chaetocnema ectypaHorn (desert corn flea beetle); C. pulicaria Melsheimer (corn fleabeetle); Colaspis brunnea Fabricius (grape colaspis); Diabrotica barberiSmith & Lawrence (northern corn rootworm); D. undecimpunctata howardiBarber (southern corn rootworm); D. virgifera virgifera LeConte (westerncorn rootworm); Leptinotarsa decemlineata Say (Colorado potato beetle);Oulema melanopus Linnaeus (cereal leaf beetle); Phyllotreta cruciferaeGoeze (corn flea beetle); Zygogramma exclamationis Fabricius (sunflowerbeetle); beetles from the family Coccinellidae including, but notlimited to: Epilachna varivestis Mulsant (Mexican bean beetle); chafersand other beetles from the family Scarabaeidae including, but notlimited to: Antitrogus parvulus Britton (Childers cane grub);Cyclocephala borealis Arrow (northern masked chafer, white grub); C.immaculata Olivier (southern masked chafer, white grub); Dermolepidaalbohirtum Waterhouse (Greyback cane beetle); Euetheola humilis rugicepsLeConte (sugarcane beetle); Lepidiota frenchi Blackburn (French's canegrub); Tomarus gibbosus De Geer (carrot beetle); T. subtropicusBlatchley (sugarcane grub); Phyllophaga crinita Burmeister (white grub);P. latifrons LeConte (June beetle); Popillia japonica Newman (Japanesebeetle); Rhizotrogus majalis Razoumowsky (European chafer); carpetbeetles from the family Dermestidae; wireworms from the familyElateridae, Eleodes spp., Melanotus spp. including M. communis Gyllenhal(wireworm); Conoderus spp.; Limonius spp.; Agriotes spp.; Cteniceraspp.; Aeolus spp.; bark beetles from the family Scolytidae; beetles fromthe family Tenebrionidae; beetles from the family Cerambycidae such as,but not limited to, Migdolus fryanus Westwood (longhorn beetle); andbeetles from the Buprestidae family including, but not limited to,Aphanisticus cochinchinae seminulum Obenberger (leaf-mining buprestidbeetle).

Adults and immatures of the order Diptera are of interest, includingleafminers Agromyza parvicornis Loew (corn blotch leafminer); midgesincluding, but not limited to: Contarinia sorghicola Coquillett (sorghummidge); Mayetiola destructor Say (Hessian fly); Neolasiopteramurtfeldtiana Felt, (sunflower seed midge); Sitodiplosis mosellana Géhin(wheat midge); fruit flies (Tephritidae), Oscinella frit Linnaeus (fritflies); maggots including, but not limited to: Delia spp. includingDelia platura Meigen (seedcorn maggot); D. coarctata Fallen (wheat bulbfly); Fannia canicularis Linnaeus, F. femoralis Stein (lesser houseflies); Meromyza americana Fitch (wheat stem maggot); Musca domesticaLinnaeus (house flies); Stomoxys calcitrans Linnaeus (stable flies));face flies, horn flies, blow flies, Chrysomya spp.; Phormia spp.; andother muscoid fly pests, horse flies Tabanus spp.; bot fliesGastrophilus spp.; Oestrus spp.; cattle grubs Hypoderma spp.; deer fliesChrysops spp.; Melophagus ovinus Linnaeus (keds); and other Brachycera,mosquitoes Aedes spp.; Anopheles spp.; Culex spp.; black fliesProsimulium spp.; Simulium spp.; biting midges, sand flies, sciarids,and other Nematocera.

Included as insects of interest are those of the order Hemiptera suchas, but not limited to, the following families: Adelgidae, Aleyrodidae,Aphididae, Asterolecaniidae, Cercopidae, Cicadellidae, Cicadidae,Cixiidae, Coccidae, Coreidae, Dactylopiidae, Delphacidae, Diaspididae,Eriococcidae, Flatidae, Fulgoridae, lssidae, Lygaeidae, Margarodidae,Membracidae, Miridae, Ortheziidae, Pentatomidae, Phoenicococcidae,Phylloxeridae, Pseudococcidae, Psyllidae, Pyrrhocoridae and Tingidae.

Agronomically important members from the order Hemiptera include, butare not limited to: Acrosternum hilare Say (green stink bug);Acyrthisiphon pisum Harris (pea aphid); Adelges spp. (adelgids);Adelphocoris rapidus Say (rapid plant bug); Anasa tristis De Geer(squash bug); Aphis craccivora Koch (cowpea aphid); A. fabae Scopoli(black bean aphid); A. gossypii Glover (cotton aphid, melon aphid); A.maidiradicis Forbes (corn root aphid); A. pomi De Geer (apple aphid); A.spiraecola Patch (spirea aphid); Aulacaspis tegalensis Zehntner(sugarcane scale); Aulacorthum solani Kaltenbach (foxglove aphid);Bemisia tabaci Gennadius (tobacco whitefly, sweetpotato whitefly); B.argentifolii Bellows & Perring (silverleaf whitefly); Blissusleucopterus leucopterus Say (chinch bug); Blostomatidae spp.;Brevicoryne brassicae Linnaeus (cabbage aphid); Cacopsylla pyricolaFoerster (pear psylla); Calocoris norvegicus Gmelin (potato capsid bug);Chaetosiphon fragaefolii Cockerell (strawberry aphid); Cimicidae spp.;Coreidae spp.; Corythuca gossypii Fabricius (cotton lace bug);Cyrtopeltis modesta Distant (tomato bug); C. notatus Distant (suckfly);Deois flavopicta Stål (spittlebug); Dialeurodes citri Ashmead (citruswhitefly); Diaphnocoris chlorionis Say (honeylocust plant bug);Diuraphis noxia Kurdjumov/Mordvilko (Russian wheat aphid);Duplachionaspis divergens Green (armored scale); Dysaphis plantagineaPaaserini (rosy apple aphid); Dysdercus suturellus Herrich-Schäffer(cotton stainer); Dysmicoccus boninsis Kuwana (gray sugarcane mealybug);Empoasca fabae Harris (potato leafhopper); Eriosoma lanigerum Hausmann(woolly apple aphid); Erythroneoura spp. (grape leafhoppers); Eumetopinaflavipes Muir (Island sugarcane planthopper); Eurygaster spp.;Euschistus servus Say (brown stink bug); E. variolarius Palisot deBeauvois (one-spotted stink bug); Graptostethus spp. (complex of seedbugs); and Hyalopterus pruni Geoffroy (mealy plum aphid); Iceryapurchasi Maskell (cottony cushion scale); Labopidicola allii Knight(onion plant bug); Laodelphax striatellus Fallen (smaller brownplanthopper); Leptoglossus corculus Say (leaf-footed pine seed bug);Leptodictya tabida Herrich-Schaeffer (sugarcane lace bug); Lipaphiserysimi Kaltenbach (turnip aphid); Lygocoris pabulinus Linnaeus (commongreen capsid); Lygus lineolaris Palisot de Beauvois (tarnished plantbug); L. Hesperus Knight (Western tarnished plant bug); L. pratensisLinnaeus (common meadow bug); L. rugulipennis Poppius (Europeantarnished plant bug); Macrosiphum euphorbiae Thomas (potato aphid);Macrosteles quadrilineatus Forbes (aster leafhopper); Magicicadaseptendecim Linnaeus (periodical cicada); Mahanarva fimbriolata Stål(sugarcane spittlebug); M. posticata Stål (little cicada of sugarcane);Melanaphis sacchari Zehntner (sugarcane aphid); Melanaspis glomerataGreen (black scale); Metopolophium dirhodum Walker (rose grain aphid);Myzus persicae Sulzer (peach-potato aphid, green peach aphid); Nasonoviaribisnigri Mosley (lettuce aphid); Nephotettix cinticeps Uhler (greenleafhopper); N. nigropictus Stål (rice leafhopper); Nezara viridulaLinnaeus (southern green stink bug); Nilaparvata lugens Stål (brownplanthopper); Nysius ericae Schilling (false chinch bug); Nysiusraphanus Howard (false chinch bug); Oebalus pugnax Fabricius (rice stinkbug); Oncopeltus fasciatus Dallas (large milkweed bug); Orthopscampestris Linnaeus; Pemphigus spp. (root aphids and gall aphids);Peregrinus maidis Ashmead (corn planthopper); Perkinsiella saccharicidaKirkaldy (sugarcane delphacid); Phylloxera devastatrix Pergande (pecanphylloxera); Planococcus citri Risso (citrus mealybug); Plesiocorisrugicollis Fallen (apple capsid); Poecilocapsus lineatus Fabricius(four-lined plant bug); Pseudatomoscelis seriatus Reuter (cottonfleahopper); Pseudococcus spp. (other mealybug complex); Pulvinariaelongata Newstead (cottony grass scale); Pyrilla perpusilla Walker(sugarcane leafhopper); Pyrrhocoridae spp.; Quadraspidiotus perniciosusComstock (San Jose scale); Reduviidae spp.; Rhopalosiphum maidis Fitch(corn leaf aphid); R. padi Linnaeus (bird cherry-oat aphid);Saccharicoccus sacchari Cockerell (pink sugarcane mealybug); Scaptocoriscastanea Perty (brown root stink bug); Schizaphis graminum Rondani(greenbug); Sipha flava Forbes (yellow sugarcane aphid); Sitobion avenaeFabricius (English grain aphid); Sogatella furcifera Horvath(white-backed planthopper); Sogatodes oryzicola Muir (rice delphacid);Spanagonicus albofasciatus Reuter (whitemarked fleahopper); Therioaphismaculata Buckton (spotted alfalfa aphid); Tinidae spp.; Toxopteraaurantii Boyer de Fonscolombe (black citrus aphid); and T. citricidaKirkaldy (brown citrus aphid); Trialeurodes abutiloneus (bandedwingedwhitefly) and T. vaporariorum Westwood (greenhouse whitefly); Triozadiospyri Ashmead (persimmon psylla); and Typhlocyba pomaria McAtee(white apple leafhopper).

Also included are adults and larvae of the order Acari (mites) such asAceria tosichella Keifer (wheat curl mite); Panonychus ulmi Koch(European red mite); Petrobia latens Müller (brown wheat mite);Steneotarsonemus bancrofti Michael (sugarcane stalk mite); spider mitesand red mites in the family Tetranychidae, Oligonychus grypus Baker &Pritchard, O. indicus Hirst (sugarcane leaf mite), O. pratensis Banks(Banks grass mite), O. stickneyi McGregor (sugarcane spider mite);Tetranychus urticae Koch (two spotted spider mite); T. mcdanieliMcGregor (McDaniel mite); T. cinnabarinus Boisduval (carmine spidermite); T. turkestani Ugarov & Nikolski (strawberry spider mite), flatmites in the family Tenuipalpidae, Brevipalpus lewisi McGregor (citrusflat mite); rust and bud mites in the family Eriophyidae and otherfoliar feeding mites and mites important in human and animal health,i.e. dust mites in the family Epidermoptidae, follicle mites in thefamily Demodicidae, grain mites in the family Glycyphagidae, ticks inthe order Ixodidae. Ixodes scapularis Say (deer tick); I. holocyclusNeumann (Australian paralysis tick); Dermacentor variabilis Say(American dog tick); Amblyomma americanum Linnaeus (lone star tick); andscab and itch mites in the families Psoroptidae, Pyemotidae, andSarcoptidae.

Insect pests of the order Thysanura are of interest, such as Lepismasaccharina Linnaeus (silverfish); Thermobia domestica Packard(firebrat).

Additional arthropod pests covered include: spiders in the order Araneaesuch as Loxosceles reclusa Gertsch & Mulaik (brown recluse spider); andthe Latrodectus mactans Fabricius (black widow spider); and centipedesin the order Scutigeromorpha such as Scutigera coleoptrata Linnaeus(house centipede). In addition, insect pests of the order Isoptera areof interest, including those of the termitidae family, such as, but notlimited to, Cornitermes cumulans Kollar, Cylindrotermes nordenskioeldiHolmgren and Pseudacanthotermes militaris Hagen (sugarcane termite); aswell as those in the Rhinotermitidae family including, but not limitedto Heterotermes tenuis Hagen. Insects of the order Thysanoptera are alsoof interest, including but not limited to thrips, such asStenchaetothrips minutus van Deventer (sugarcane thrips).

Embodiments of the present invention are further defined in thefollowing Examples. It should be understood that these Examples aregiven by way of illustration only. From the above discussion and theseExamples, one skilled in the art can ascertain the essentialcharacteristics of this invention, and without departing from the spiritand scope thereof, can make various changes and modifications of theembodiments of the invention to adapt it to various usages andconditions. Thus, various modifications of the embodiments of theinvention, in addition to those shown and described herein, will beapparent to those skilled in the art from the foregoing description.Such modifications are also intended to fall within the scope of theappended claims.

The disclosure of each reference set forth herein is incorporated hereinby reference in its entirety.

EXAMPLES Example 1 Transformation of Maize by AgrobacteriumTransformation and Regeneration of Transgenic Plants Containing theCry1F, Cry34Ab1, Cry35Ab1 (Cry34/35Ab1) and Pat Genes

4114 maize was produced by Agrobacterium-mediated transformation withplasmid PHP27118. This event contains the cry1F, cry34Ab1, cry35Ab1, andpat gene cassettes, which confer resistance to certain lepidopteran andcoleopteran pests.

Specifically, the first cassette contains a truncated version of thecry1F gene from Bt var. aizawai. The insertion of the cry1F gene confersresistance to damage by lepidopteran pests, including ECB and FAW. TheCry1F protein (SEQ ID NO: 1) is comprised of 605 amino acids and has amolecular weight of approximately 68 kDa. The expression of the cry1Fgene is controlled by the maize polyubiquitin promoter (Christensen etal., 1992, supra), providing constitutive expression of Cry1F protein inmaize. This region also includes the 5′ UTR and intron associated withthe native polyubiquitin promoter. The terminator for the cry1F gene isthe poly(A) addition signal from open reading frame 25 (ORF 25) of theAgrobacterium tumefaciens (A. tumefaciens) Ti plasmid pTi15955 (Barkeret al., 1983, supra).

The second cassette contains the cry34Ab1 gene isolated from Bt strainPS149B1 (U.S. Pat. Nos. 6,127,180; 6,624,145 and 6,340,593). TheCry34Ab1 protein (SEQ ID NO: 2) is 123 amino acid residues in length andhas a molecular weight of approximately 14 kDa. The expression of thecry34Ab1 gene is controlled by a second copy of the maize polyubiquitinpromoter with 5′ UTR and intron (Christensen et al., 1992, supra). Theterminator for the cry34Ab1 gene is the pinII terminator (Keil et al.,1986, supra; An et al., 1989, supra).

The third gene cassette contains the cry35Ab1 gene, also isolated fromBt strain PS149B1 (U.S. Pat. Nos. 6,083,499; 6,548,291 and 6,340,593).The Cry35Ab1 protein (SEQ ID NO: 3) has a length of 383 amino acids anda molecular weight of approximately 44 kDa. Simultaneous expression ofthe Cry34Ab1 and Cry35Ab1 proteins in the plant confers resistance tocoleopteran insects, including WCRW. The expression of the cry35Ab1 geneis controlled by the Triticum aestivum (wheat) peroxidase promoter andleader sequence (Hertig et al. 1991, supra). The terminator for thecry35Ab1 gene is a second copy of the pinII terminator (Keil et al.1986, supra; An et al. 1989, supra).

The fourth and final gene cassette contains a version of pat fromStreptomyces viridochromogenes that has been optimized for expression inmaize. The pat gene expresses PAT, which confers tolerance tophosphinothricin (glufosinate-ammonium). The PAT protein (SEQ ID NO: 4)is 183 amino acids residues in length and has a molecular weight ofapproximately 21 kDa. Expression of the pat gene is controlled by thepromoter and terminator regions from the CaMV 35S transcript (Franck etal., 1980, supra; Odell et al., 1985, supra; Pietrzak, et al., 1986,supra). Plants containing the DNA constructs are also provided. Adescription of the genetic elements in the PHP27118 T-DNA (set forth inSEQ ID NO: 5) and their sources are described further in Table 1.

TABLE 1 Genetic Elements in the T-DNA Region of Plasmid PHP27118Location on T-DNA (bp Genetic Size position) Element (bp) Description  1to 25 Right 25 T-DNA RB region from Ti plasmid Border of A. tumefaciens26 to 76 Ti Plasmid 51 Non-functional sequence from Ti plasmid of A.Region tumefaciens  77 to 114 Polylinker 38 Region required for cloninggenetic elements Region  115 to 1014 ubiZM1 900 Promoter region from Zeamays polyubiquitin Promoter gene (Christensen et al., 1992, supra) 1015to 1097 ubiZM1 5′ 83 5′ UTR from Zea mays polyubiquitin gene. Id. UTR1098 to 2107 ubiZM1 1010 Intron region from Zea mays polyubiquitinIntron gene. Id. 2108 to 2129 Polylinker 22 Region required for cloninggenetic elements Region 2130 to 3947 cry1F Gene 1818 Truncated versionof cry1F from Bt var. aizawai 3948 to 3992 Polylinker 45 Region requiredfor cloning genetic elements Region 3993 to 4706 ORF 25 714 Terminatorsequence from A. tumefaciens Terminator pTi15955 ORF 25 (Barker et al.,1983, supra) 4707 to 4765 Polylinker 59 Region required for cloninggenetic elements Region 4766 to 5665 ubiZM1 900 Promoter region from Zeamays polyubiquitin Promoter gene (Christensen et al., 1992, supra) 5666to 5748 ubiZM1 5′ 83 5′ UTR from Zea mays polyubiquitin gene. Id. UTR5749 to 6758 ubiZM1 1010 Intron region from Zea mays polyubiquitinIntron gene. Id. 6759 to 6786 Polylinker 28 Region required for cloninggenetic elements Region 6787 to 7158 cry34Ab1 372 Synthetic version ofcry34Ab1 encoding 14 kDa Gene delta-endotoxin parasporal crystal proteinfrom the nonmotile strain PS149B1 of Bt (Moellenbeck et al. (2001)Nature Biotech. 19:668-672; Ellis et al. (2002) Appl. Env. Microbiol.68(3):1137-1145; Herman et al. (2002) Environ. Entomol. 31(2):208-214.)7159 to 7182 Polylinker 24 Region required for cloning genetic elementsRegion 7183 to 7492 pinII 310 Terminator region from Solanum tuberosumTerminator proteinase inhibitor II gene (Keil et al. 1986, supra; An etal. 1989, supra) 7493 to 7522 Polylinker 30 Region required for cloninggenetic elements Region 7523 to 8820 TA 1298 Promoter from Triticumaestivum peroxidase Peroxidase including leader sequence (Hertig et al.1991, Promoter supra) 8821 to 8836 Polylinker 16 Region required forcloning genetic elements Region 8837 to 9988 cry35Ab1 1152 Syntheticversion of cry35Ab1 encoding a 44 kDa delta-endotoxin parasporal crystalprotein from the nonmotile strain PS149B1 of Bt (Moellenbeck et al.2001, supra; Ellis et al. 2002, supra; Herman et al. 2002, supra)  9989to 10012 Polylinker 24 Region required for cloning genetic elementsRegion 10013 to 10322 pinII 310 Terminator region from Solanum tuberosumTerminator proteinase inhibitor II gene (Keil et al. 1986, supra; An etal. 1989, supra) 10323 to 10367 Polylinker 45 Region required forcloning genetic elements Region 10368 to 10897 CaMV 530 35S promoterfrom CaMV (Franck et al., 1980, 35S supra; Odell et al., 1985, supra;Pietrzak, Promoter et al., 1986, supra) 10898 to 10916 Polylinker 19Region required for cloning genetic Region elements 10917 to 11468 patGene 552 Synthetic, plant-optimized phosphinothricin acetyltransferasecoding sequence from Streptomyces viridochromogenes. 11469 to 11488Polylinker 20 Region required for cloning genetic Region elements 11489to 11680 CaMV35S 192 35S terminator from CaMV (Franck et al., Terminator1980, supra; Pietrzak, et al., 1986, supra) 11681 to 11756 Polylinker 76Region required for cloning genetic elements Region 11757 to 11953 TiPlasmid 197 Non-functional sequence from Ti plasmid of Region A.tumefaciens 11954 to 11978 Left Border 25 T-DNA LB region from Tiplasmid of A. tumefaciens

Immature embryos of maize (Zea mays L.) were aseptically removed fromthe developing caryopsis nine to eleven days after pollination andinoculated with A. tumefaciens strain LBA4404 containing plasmidPHP27118 (FIG. 1), essentially as described in Zhao (U.S. Pat. No.5,981,840, the contents of which are hereby incorporated by reference).The T-DNA region of PHP27118 is shown in FIG. 2. After three to six daysof embryo and Agrobacterium co-cultivation on solid culture medium withno selection, the embryos were then transferred to a medium withoutherbicide selection but containing carbenicillin. After three to fivedays on this medium, embryos were then transferred to selective mediumthat was stimulatory to maize somatic embryogenesis and containedbialaphos for selection of cells expressing the pat transgene. Themedium also contained carbenicillin to kill any remaining Agrobacterium.After six to eight weeks on the selective medium, healthy, growing callithat demonstrated resistance to bialaphos were identified. The putativetransgenic calli were subsequently regenerated to produce T0 plantlets.

Samples were taken from the T0 plantlets for PCR analysis to verify thepresence and copy number of the inserted cry1F, cry35Ab1, cry34Ab1,and/or pat genes. Maize event DP-004114-3 was confirmed to contain asingle copy of the T-DNA (See Examples 2 and 3). In addition to thisanalysis, the T0 plantlets were analyzed for the presence of certainAgrobacterium binary vector backbone sequences by PCR (data not shown).Plants that were determined to be single copy for the inserted genes andnegative for Agrobacterium backbone sequences were selected for furthergreenhouse propagation. These selected T0 plants were screened for traitefficacy and protein expression by conducting numerous bioassays (SeeExample 5). The T0 plants meeting all criteria were advanced and crossedto inbred lines to produce seed for further testing. A schematicoverview of the transformation and event development is presented inFIG. 3.

Example 2 Characterization of Maize Event DP-004114-3

Genomic DNA from leaf tissue of test seed from 4114 maize and a controlsubstance (seed from a non-genetically modified maize with a geneticbackground representative of the event background) was isolated andsubjected to qualitative PCR amplification using a construct-specificprimer pair. The PCR products were separated on an agarose gel toconfirm the presence of the inserted construct in the genomic DNAisolated from the test seed, and the absence of the inserted constructin the genomic DNA isolated from the control seed. A reference standard(Low DNA Mass Ladder; Invitrogen Corporation Catalog #10380-012) wasused to determine the PCR product size. The reliability of theconstruct-specific PCR method was assessed by repeating the experimentthree times. The sensitivity of the PCR amplification was evaluated byvarious dilutions of the genomic DNA from 4114 maize.

Test and control leaf samples (V5-V7 leaf stage) were harvested fromplants grown at the DuPont Experimental Station (Wilmington, Del.) fromseed obtained from Pioneer Hi-Bred (Johnston, Iowa). Genomic DNAextractions from the test and control leaf tissues were performed usinga standard urea extraction protocol.

Genomic DNA was quantified using the NanoDrop 1000 Spectrophotometerusing ND-1000 V3.6 Software (ThermoScientific, Wilmington, Del.) and theQuant-iT PicoGreen® reagent (Invitrogen, Carslbad, Calif.). DNA sampleswere visualized on an agarose gel to confirm quantitation values and todetermine the DNA quality.

Genomic DNA samples isolated from leaf tissue of 4114 maize and controlsamples were subjected to PCR amplification (Roche High Fidelity PCRMaster Kit, Roche Catalog #12140314001) utilizing a construct-specificprimer pair (SEQ ID NOs: 7 and 8) which spans the maize ORF 25terminator and the ubiquitin promoter (See FIG. 2), and allows for theunique identification of the inserted T-DNA in 4114 maize. A secondprimer set (SEQ ID NOs: 9 and 10) was used to amplify the endogenousmaize invertase gene (GenBank accession number AF171874.1) as a positivecontrol for PCR amplification. The PCR target site and size of theexpected PCR product for each primer set are shown in Table 2. PCRreagents and reaction conditions are shown in Table 3. In this study, 50ng of leaf genomic DNA was used in all PCR reactions.

TABLE 2 PCR Genomic DNA Target Site and Expected Size of PCR ProductsExpected Size of Primer Set Target Site PCR Product (bp) SEQ ID NO: 7 &8 Construct Specific T-DNA: 287 ORF 25 terminator and ubiquitin promoterSEQ ID NO: 9 & 10 Endogenous maize 225 invertase gene

TABLE 3 PCR Reagents and Reaction Conditions PCR Reagents PCR ReactionConditions Volume Cycle Temp Time # Reagent (μL) Element (° C.) (sec)Cycles Template DNA 2 Initial 94 120 1 (25 ng/μL) Denaturation Primer 1(10 μM) 2 Denaturation 94 10 35 Primer 2 (10 μM) 2 Annealing 65 15 PCRMaster Mix* 25 Elongation 68 60 ddH₂O 19 Final Elongation 68 420 1 — —Hold Cycle 4 Until — analysis ddH₂O: double-distilled water *Roche HighFidelity Master Mix

A PCR product of approximately 300 bp in size amplified by theconstruct-specific primer set (SEQ ID NOs: 7 and 8) was observed in PCRreactions using plasmid PHP27118 (10 ng) as a template and all 4114maize DNA samples, but absent in all control maize samples and theno-template control. This experiment was repeated three times, andsimilar results were obtained. Results observed for DNA extracts fromfive 4114 maize plants and five control maize plants correspondedclosely with the expected PCR product size (287 bp) for samplescontaining 4114 maize genomic DNA. A PCR product approximately 220 bp insize was observed for both 4114 maize and control maize samplesfollowing PCR reaction with the primer set (SEQ ID NOs: 9 and 10) fordetection of the endogenous maize invertase gene. These resultscorresponded closely with the expected PCR product size (225 bp) forgenomic DNA samples containing the maize endogenous invertase gene. Theendogenous target band was not observed in the no-template control.

In order to assess the sensitivity of the PCR amplification, variousconcentrations of a single DNA sample from 4114 maize were diluted innon-genetically modified control DNA, resulting in 4114 maize DNAamounts ranging from 500 fg, 5 pg, 10 pg, 50 pg, 100 pg, 5 00 pg, 5 ng,and 50 ng (the total amount of genomic DNA in all PCR samples was 50ng). Each dilution was subjected to PCR amplification as previouslyconducted. Based on this analysis, the limit of detection (LOD) wasdetermined to be approximately 100 pg of 4114 maize DNA in 50 ng oftotal DNA, or 0.2% 4114 maize DNA.

In conclusion, qualitative PCR analysis utilizing a construct-specificprimer set for 4114 maize confirmed that the test plants contained theinserted T-DNA from plasmid PHP27118, as evident by the presence of theconstruct-specific target band in all test plant samples analyzed, andthe absence in the non-genetically modified control plants. This resultwas reproducible. Test and control plants both contained the endogenousmaize invertase gene. The sensitivity of the analysis under theconditions described is approximately 100 pg of 4114 maize genomic DNAin 50 ng of total genomic DNA or 0.2% 4114 maize genomic DNA.

Example 3 Southern Blot Analysis of DP-004114-3 maize for Integrity andCopy Number

Southern blot analysis was used to confirm the integrity and copy numberof the inserted T-DNA from PHP27118 and to confirm the presence of thecry1F, cry34Ab1, cry35Ab1, and pat gene cassettes in 4114 maize.

Five individual plants from the T1 generation of 4114 maize wereselected for Southern blot analysis. Young leaf material was harvestedfrom the 4114 maize (test) and non-transgenic maize (control) plants andwas immediately placed on dry ice. The frozen samples were lyophilizedand genomic DNA was extracted from the test and control tissues using aCTAB extraction method.

Following restriction enzyme digestions as detailed below, the DNAfragments were separated on agarose gels, depurinated, denatured, andneutralized in situ, and transferred to a nylon membrane in 20×SSCbuffer using the method as described for TURBOBLOTTER™ Rapid DownwardTransfer System (Schleicher & Schuell). Following transfer to themembrane, the DNA was bound to the membrane by ultraviolet lightcrosslinking.

Integrity

The restriction enzyme Hind III was selected for Southern analysis ofintegrity, as there are three sites located within the T-DNA (FIG. 2).Approximately 1-3 μg of genomic DNA was digested with Hind III andseparated by size on an agarose gel. As a positive control,approximately 15 pg of plasmid containing the PHP27118 T-DNA was spikedinto a control plant DNA sample, digested and included on the agarosegel. A negative control was also included to verify backgroundhybridization of the probe to the maize genome.

Four probes homologous to the cry1F, cry34Ab1, cry35Ab1, and pat geneson the PHP27118 T-DNA (for gene elements, see FIG. 2) were used forhybridization to confirm the presence of the genes. In order to developthe probes, fragments homologous to the cry1F, cry34Ab1, cry35Ab1, andpat genes were generated by PCR from plasmid containing the PHP27118T-DNA, size separated on an agarose gel, and purified using a QIAquick®gel extraction kit (Qiagen). All DNA probes were subsequently generatedfrom the fragments using the Rediprime™ II DNA Labeling System(Amersham) which performs random prime labeling with [³²P]dCTP.

The labeled probes were hybridized to the target DNA on the nylonmembranes for detection of the specific fragments using the MiracleHyb®Hybridization Solution essentially as described by the manufacturer(Stratagene). Washes after hybridization were carried out at highstringency. Blots were exposed to X-ray film at −80° C. for one or moretime points to detect hybridizing fragments.

Because the Hind III enzyme sites were known within the T-DNA, exactexpected band sizes were determined for each of the probes (Table 4,FIG. 2). For an intact copy of the T-DNA, the cry1F probe was expectedto hybridize to a fragment of 3891 bp. The cry34Ab1, cry35Ab1, and patgene probes were expected to hybridize to a fragment of 7769 bp.Fragments from the test samples matching the expected sizes, as well asmatching the bands in the plasmid control sample, would confirm theintegrity of the inserted T-DNA and the presence of each gene.

The results of the Southern blot analysis with Hind III and the cry1F,cry34Ab1, cry35Ab1, and pat gene probes confirmed the expected fragmentsizes and, thus, confirmed that the T-DNA inserted intact into each ofthe events and that each of the genes was present.

A band of approximately 4 kb was observed with the cry1F probe which isconsistent with the expected fragment size. A similar fragment ofapproximately 4 kb was observed in the plasmid positive control lane,which was presumed to be the expected band of 3891 bp. Based onequivalent migration of the hybridizing band in the events to the bandin the plasmid positive control, it was confirmed that the portion ofthe T-DNA containing cry1F had inserted intact in 4114 maize.

In the hybridization with the cry34Ab1 probe, a band of approximately 8kb was observed in the event and also in the plasmid positive control.The hybridizing band in the plasmid positive control lane was presumedto be the expected band of 7769 bp. Because the hybridizing band in theevent had migrated equivalently with this band, it was confirmed thatthis portion of the T-DNA containing cry34Ab1 was inserted intact.

Similarly, hybridizations with cry35Ab1 and pat hybridized to the same7769 bp fragment in the plant and plasmid positive control as expected.These results confirmed that the portion of the T-DNA containing thecry35Ab1 and pat genes had inserted intact.

This Southern blot analysis confirms that 4114 maize contains an intactcopy of the T-DNA from PHP27118 containing the cry1F, cry34Ab1,cry35Ab1, and pat genes.

TABLE 4 Summary of Expected and Observed Hybridization Fragments onSouthern Blots for 4114 Maize DNA digested with Hind III ExpectedFragment Size from Observed Fragment Probe PHP27118 T-DNA (bp)¹ Size(kb) ² cry1F 3891 ~4 cry34Ab1 7769 ~8 cry35Ab1 7769 ~8 pat 7769 ~8¹Expected fragment sizes based on map of PHP27118 T-DNA (FIG. 2). ² Allobserved fragments migrated equivalently with the plasmid positivecontrol and, therefore, were confirmed to represent the intact portionof the PHP27118 T-DNA.

Copy Number

The cry1F and pat probes were used in Southern blot hybridizations toevaluate the copy number of the insertions in 4114 maize.

The restriction enzyme Bcl I was selected for Southern analysis of copynumber, as there is a single site located within the T-DNA (FIG. 2).Approximately 3 μg of genomic DNA from individual plants of the T1generation of event 4114 was digested with Bcl I and separated by sizeon an agarose gel. A plasmid containing the PHP27118 T-DNA was spikedinto a control plant DNA sample, digested and included on the agarosegel to serve as a positive hybridization control. Negative control maizeDNA was also included to verify background hybridization of the probe tothe maize genome. DNA Molecular Weight Marker VII, digoxigenin (DIG)labeled (Roche, Indianapolis, Ind.), was included on Bcl I blots as asize standard for hybridizing fragments.

Probes for the cry1F and pat genes were also labeled by a PCR reactionincorporating a digoxigenin (DIG) labeled nucleotide, [DIG-11]-dUTP,into the fragment. PCR labeling of isolated fragments was carried outaccording to the procedures supplied in the PCR DIG Probe Synthesis Kit(Roche).

The DIG-labeled probes were hybridized to the Bcl I Southern blots ofthe T1 generation of the 4114 event. Probes were hybridized to thetarget DNA for detection of the specific fragments using DIG Easy Hybsolution (Roche) essentially as described by manufacturer.Post-hybridization washes were carried out at high stringency.DIG-labeled probes hybridized to the bound fragments were detected usingthe CDP-Star Chemiluminescent Nucleic Acid Detection System (Roche).Blots were exposed to X-ray film at room temperature for one or moretime points to detect hybridizing fragments. Membranes were stripped ofhybridized probe following the manufacturer's recommendation prior tohybridization with additional probes.

The restriction enzyme Bcl I, having a single restriction site withinthe T-DNA (FIG. 2), was selected to confirm the presence of a singlePHP27118 T-DNA insertion in 4114 maize. The site for Bcl I is located atby 2546 of the T-DNA (FIG. 2) and will yield fragments of greater thanabout 2500 bp and 9400 bp for a single inserted T-DNA. Hybridizationwith the pat probe would indicate the number of copies of this elementfound in the event based on the number of hybridizing bands (e.g., onehybridizing band indicates one copy of the element). The pat probe wouldhybridize to the fragment of greater than 9400 bp. Because the Bcl Irestriction enzyme site is within the cry1F gene, the cry1F probe isexpected to hybridize to both fragments and result in two bands for asingle T-DNA insertion (FIG. 2).

The results of the Southern blot analysis with Bcl I and the cry1F andpat gene probes for 4114 maize are summarized in Table 5.

TABLE 5 Summary of Expected and Observed Hybridization Fragments onSouthern Blots for Bcl I digests of 4114 Maize Expected FragmentObserved Size from Fragment Enzyme PHP27118 Size Probe Digest T-DNA(bp)¹ (kb)² cry1F Bcl I  >2500³ ~3.1 >9400 >8.6 pat Bcl I >9400 >8.6¹Expected fragment sizes based on map of PHP27118 T-DNA (Figure 2). ²Allobserved fragment sizes are approximated based on the migration of theDIG VII molecular weight marker. ³Two fragments are expected with thecry1F probe due to the location of the Bcl I restriction site within thecry1F gene.

The results of the Southern blot analysis of 4114 maize with Bcl Idigestion and the cry1F probe showed two bands as expected, one band ofgreater than 8.6 kb and a second band of approximately 3.1 kb. Two bandsare expected for a single insertion due to the location of the Bcl Isite within the cry1F gene, so these results indicate that there is asingle copy of cry1F in 4114 maize. The results of the Southern blotanalysis of 4114 maize with Bcl I digestion and the pat probe showed asingle band of greater than 8.6 kb that matched the size of the largercry1F band as expected. These results indicate that there is also asingle insertion of the pat gene in maize event 4114.

As the cry34Ab1 and cry35Ab1 genes are located on the same fragment asthe pat gene and part of the cry1F gene, and between the cry1F and patgenes on the T-DNA, by extension this also demonstrates that this eventis likely to contain a single copy of each of these genes.

Example 4 Sequencing Characterization of Insert and Genomic BorderRegions of Maize Event DP-004114-3

The sequence of the insert and genomic border regions was determined toconfirm the integrity of the inserted DNA and to characterize thegenomic sequence flanking the insertion site present in 4114 maize. Intotal, 16,752 bp of 4114 maize genomic sequence was confirmed,comprising 2,422 bp of the 5′ genomic border sequence, 2,405 bp of the3′ genomic border sequence, and 11,925 bp of inserted T-DNA fromPHP27118. The inserted T-DNA in 4114 maize was found to have a 29 bpdeletion on the Right Border (RB) end and a 24 bp deletion on the LeftBorder (LB) end. All remaining sequence is intact and identical to thatof plasmid PHP27118. The 5′ and 3′ genomic border regions of 4114 maizewere verified to be of maize origin by PCR amplification and sequencingof the genomic border regions from both 4114 maize and control maizeplants.

Seed containing event DP-004114-3 was obtained from a T1S2 generation of4114 maize. Control seed was obtained from a maize line that has asimilar genetic background to 4114 maize but does not contain the cry1F,cry34Ab1, cry35Ab1, and pat gene cassettes. All seeds were obtained fromPioneer Hi-Bred International, Inc. (Johnston, Iowa). The Low DNA MassLadder (Invitrogen Corp., Carlsbad, Calif.) and the High DNA Mass Ladder(Invitrogen Corp.) were used for gel electrophoresis to estimate DNAfragment sizes on agarose gels.

The 4114 maize seed and the control seed were planted in growth chambersat the DuPont Experimental Station (Wilmington, Del.) to produce planttissues used for this study. One seed was planted per pot, and the potwas uniquely identified. All plants were grown with light, temperature,and water regulated for healthy plant growth. Leaf samples werecollected from the control and 4114 maize plants. For each individualplant, leaf material was collected in a pre-labeled bag, placed on dryice, and then transferred to an ultra low freezer (<−55° C.) followingcollection. All samples were maintained frozen until tissue processing.

Genotype Confirmation via Event-Specific PCR Analysis

A leaf sample was taken from all test and control plants forevent-specific PCR analysis. DNA was extracted from each leaf sampleusing the Extract-N-Amp™ Plant PCR kit following the described procedure(Sigma-Aldrich, St. Louis, Mo.) for real-time PCR analysis.

Real-time PCR was performed on each DNA sample utilizing an ABI PRISM®7500HT Sequence Detection System (Applied Biosystems, Inc., Foster City,Calif.). TaqMan® probe (Applied Biosystems, Inc.) and primer sets(Integrated DNA Technologies, Coralville, Iowa) were designed to detecta target sequence from 4114 maize. In addition, a second TaqMan® probeand primer set for a reference maize endogenous gene was used to confirmthe presence of amplifiable DNA in each reaction. The analysis consistedof real-time PCR determination of qualitative positive/negative calls.The extracted DNA was assayed using TaqMan® Universal PCR Master Mix, NoAmpErase® UNG (Applied Biosystems, Inc.).

Positive or negative determination for 4114 maize was based oncomparison of the CT (threshold cycle) of the event-specific target PCRto that of the maize endogenous reference target. If the event andendogenous PCR targets amplified above CT threshold, then the plant wasscored as positive for that event. If the endogenous target amplifiedand the event target did not, then the plant was scored as negative. Ifneither target amplified for a particular sample, then it was determinedto be a poor quality DNA sample or failed run and the assay wasrepeated.

All 4114 maize plants were positive for the event-specific PCR and thePAT, Cry1F, and Cry34Ab1 proteins, whereas all the control maize plantswere negative. The results are summarized in Table 6.

TABLE 6 Summary of Event-Specific PCR Analysis and Cry1F, Cry34Ab1, andPAT Protein Expression in 4114 Maize and Control Maize Plants Event-Specific 4114 Maize Plant ID PCR¹ Cry1F² Cry34Ab1² PAT²T-F-08-233C-1 + + + + T-F-08-233C-2 + + + + T-F-08-233C-3 + + + +T-F-08-233C-4 + + + + Control Maize Plant ID C-F-08-246C-1 − − − −C-F-08-246C-2 − − − − ¹Summary of event-specific real time PCR assay for4114 maize. Positive (+) indicates the presence of 4114 maize event.Negative (−) indicates the absence of 4114 maize event. ²Summary ofCry1F, Cry34Ab1, and PAT protein expression in 4114 maize and controlmaize plants using lateral flow devices. Positive (+) indicates thepresence of the protein. Negative (−) indicates the absence of theprotein.

DNA Sequencing

DNA fragments were cloned and submitted for sequencing at the PioneerCrop Genetics Research sequencing facility (Wilmington, Del.).Sequencher™ software from Gene Codes Corporation (Ann Arbor, Mich.) wasused to assemble the sequences. Sequence annotation was performed usingVector NTI 9.1.0 (Invitrogen Corp) by comparing the T-DNA insertsequences generated from 4114 maize with the sequences from the T-DNAregion of plasmid PHP27118 (used for transformation to produce 4114maize).

The T-DNA region of plasmid PHP27118, used to create 4114 maize, wassequenced and compared with the inserted T-DNA sequence in 4114 maize.

The sequence of the T-DNA region of plasmid PHP27118 was used to designprimer pairs to characterize the inserted T-DNA in 4114 maize. Sixoverlapping PCR products were generated using genomic DNA from fourdifferent 4114 maize plants as template. These PCR products were clonedand sequenced.

Sequencing of 5′ and 3′ Flanking Genomic Border Regions

Preliminary sequence characterization of the 5′ and 3′ flanking genomicborder regions were carried out using several rounds of inverse PCR,(Silver and Keerikatte (1989) J. Virol. 63: 1924; Ochman et al. (1988)Genetics 120:621-623; Triglia et al., (1988) Nucl. Acids Res. 16:8186)with primers anchored within various regions of the inserted T-DNA.Sequence information obtained from inverse PCR was subjected to BLASTnanalysis and showed a match to the maize BAC clone AC211214 from theNCBI (National Center for Biotechnology Information) GenBank nucleotidedatabase. This sequence was then used to design primers that spanned the5′ and 3′ insert/genomic junctions in 4114 maize. The PCR productsgenerated from four 4114 maize plants were cloned and sequenced toverify the 5′ and 3′ insert/genomic junctions and the genomic borderregions.

In addition, to demonstrate that the identified 5′ and 3′ genomic borderregions were of maize origin, PCR was performed on 4114 maize andcontrol maize plants within the genomic regions. Each PCR fragment wasdirectly sequenced to verify its identity of maize origin.

The T-DNA sequence information of plasmid PHP27118 was used to designprimers to verify the inserted sequence in 4114 maize (Tables 7 and 8).

TABLE 7 PCR Primers Used to Characterize the Genomic Border Regions andInserted T-DNA in 4114 Maize PCR Primer Primer SEQ Size AmplifiedFragment Pair ID NOs: (bp) Region A 09-0-3030/ 11/12 2511 5′ Genomicborder 09-0-2787 region and insert B 09-0-3036/ 13/14 3622 Insert09-0-3046 C 09-0-2980/ 16/15 4146 Insert 09-0-3045 D 08-0-2463/ 17/182713 Insert 08-0-2759 E 09-0-2775/ 19/20 3062 Insert 09-0-3083 F09-0-2799/ 21/22 2612 3′ Genomic border 09-0-3005 region and insert G09-0-3230/ 23/24 257 5′ Genomic border 09-0-3229 region H 09-0-3231/25/26 283 3′ Genomic border 09-0-3084 region

TABLE 8 Sequence and Location of Primers Used For PCR Reactions. TargetPrimer Sequence PCR (SEQ ID Location Fragment NO:) Primer Sequence (5′- 3′) (bp to bp)¹ A 09-0-3030 GAGCATATCCAGCACCAGCTGGTACCAAG  1-29(SID: 11) 09-0-2787 GCAGGCATGCCCGCGGATA 2,511-2,493 (SID: 12) B09-0-3036 TGGTCTACCCGATGATGTGATTGGCC 1,994-2,019 (SID: 13) 09-0-3046CGAAGACAGGATCTGACAAGGTCCGATAG 5,615-5,587 (SID: 14) C 09-0-3045GACTTCATGAACTCTTTGTTTGTGACTGCAGAGAC 5,414-5,414 (SID: 15) 09-0-2980CTCATGACTCAGGACTTGTGGC 9,559-9,538 (SID: 16) D 08-0-2463ATCAGCCTCTACTTCGAC 9,390-9,407 (SID: 17) 08-0-2759CTCCATGATCTTCGTCTCATGTG 12,102-12,080 (SID: 18) E 09-0-2775CACCAACTCCATCCAGAAGTGGC 11,481-11,503 (SID: 19) 09-0-3083GCCTTGCATTGGCGCAGTGAGAACCG 14,542-14,517 (SID: 20) F 09-0-2799CGGCGCGCCTCTAGTTGAAGACACGTT 14,141-14,167 (SID: 21) 09-0-3005CACTGGACTGAGCCGCACAGCTAAGGACAC 16,752-16,723 (SID: 22) G 09-0-3230GGAACATTCAGACTTGGGAGTCTGGACT 2,086-2,113 (SID: 23) 09-0-3229GAACAGGGTCCTCGAATCAAGGGCAGC 2,342-2,316 (SID: 24) H 09-0-3231CGGTTCTCACTGCGCCAATGCAAGGC 14,517-14,542 (SID: 25) 09-0-3084CATGACGACCATGAAGCAACATC 14,799-14,777 (SID: 26) ¹Location in sequence of4114 Maize. Bases 1 - 2,422 = 5′ genomic border region Bases 2,423 -14,347 = insert Bases 14,348 - 16,752 = 3′ genomic border region.

To characterize the inserted T-DNA in 4114 maize, PCR primers weredesigned to amplify the T-DNA insert in six separate, overlapping PCRproducts as outlined in Table 7: fragments A through F (Positionsindicated in FIG. 5). As expected, the predicted PCR products weregenerated only from 4114 maize genomic DNA samples, and were not presentin the control maize samples. The six PCR products were cloned andsequenced. When comparing the sequence of the inserted T-DNA in 4114maize to the T-DNA region of plasmid PHP27118 used to create 4114 maize,it was determined that there was a 29 bp deletion on the RB end, and a24 bp deletion on the LB end. RB and LB termini deletions often occur inAgrobacterium-mediated transformation (Kim et al. (2007) Plant J.51:779-791). All remaining sequence is intact and identical to that ofplasmid PHP27118. The sequence of the insertion is presented in SEQ IDNO: 27.

To verify the additional 5′ genomic border sequence, PCR was performedwith a forward primer (SEQ ID NO: 11) in the 5′ genomic border regionand a reverse primer (SEQ ID NO: 12) within the inserted T-DNA. Theresulting 2,511 bp PCR fragment A from 4114 maize genomic DNA sampleswas cloned and sequenced (FIG. 3). The 2,422 bp of the 5′ genomic borderregion sequence is set forth in nucleotides 1-2,422 of SEQ ID NO: 27.

To verify the additional 3′ genomic border sequence, PCR was performedwith a forward primer (SEQ ID NO: 21) within the inserted T-DNA and areverse primer (SEQ ID NO: 22) in the 3′ genomic border region. Theresulting 2,612 bp PCR fragment F from 4114 maize genomic DNA sampleswas cloned and sequenced (FIG. 3). The 2,405 bp of the 3′ genomic borderregion sequence is set forth in nucleotides 14,348 to 16,752 of SEQ IDNO: 27.

In total, 16,752 bp of sequence from genomic DNA of 4114 maize wereconfirmed: 2,422 bp of the 5′ genomic border sequence, 2,405 bp of the3′ genomic border sequence, and 11,925 bp comprising the inserted T-DNA.

To demonstrate that the identified 5′ and 3′ flanking genomic bordersequences are of maize origin, PCR was performed within the 5′ and 3′genomic border regions (the primer pair set forth in SEQ ID NOs: 23 and24 and the primer pair set forth in SEQ ID NOs: 25 and 26, respectively)on 4114 maize genomic DNA samples and control maize samples. Theexpected PCR fragment G (257 bp for the 5′ genomic region) and PCRfragment H (283 bp for the 3′ genomic region) were generated from both4114 maize and control maize. These PCR products were cloned andsequenced, and the corresponding products from the 4114 maize and thecontrol maize are identical, thus confirming that the sequences are ofmaize genomic origin.

Example 5 Insect Efficacy of Maize Event DP-004114-3

Efficacy data was generated on 4114 maize. Field testing compared 4114maize in two genetic backgrounds to a negative control (isoline) in thesame backgrounds. Efficacy testing included: first generation ECB (ECB1)foliage damage and second generation ECB (ECB2) stalk damage at fourlocations, WCRW root damage at three locations, and FAW foliar damage atone location. At each location, single-row plots were planted in arandomized complete block with three replications (20 kernels/plot×12entries×3 replicates=1 experiment/location). All plants were tissuesampled after emergence to confirm the presence of the event byevent-specific PCR. Any negatives were culled and each plot thinned to atarget stand of 10-15 evenly spaced plants per plot.

For trials characterizing ECB1 damage, each plant was manually infestedwith approximately 100 ECB neonate larvae 3 times (300 larvae total)over approximately one week beginning at approximately the V5 growthstage. Approximately three weeks after the last successful infestation,leaf damage ratings (based on a 9-1 visual rating scale where 9indicates no damage and 1 indicates maximum damage) were taken on 8consecutive plants per plot (total of 24 plants per genetic background,per entry) and means were calculated for each treatment. Firstgeneration ECB foliar feeding results on 4114 maize are shown in Table9.

TABLE 9 Efficacy of DP-004114-3 Maize Against First Generation ECBLarvae Mean ECB1LF Damage Rating ± Location Maize Line Standard Error^(a,b) York, NE 4114 9.0 ± 0.05 A 1507 × 59122 9.0 ± 0.08 A Negativecontrol 4.4 ± 0.09 B Johnston, IA 4114 9.0 ± 0.00 A 1507 × 59122 9.0 ±0.00 A Negative control 4.5 ± 0.08 B Mankato, MN 4114 9.0 ± 0.02 A 1507× 59122 9.0 ± 0.03 A Negative control 4.7 ± 0.11 B Princeton, IL 41149.0 ± 0.00 A 1507 × 59122 9.0 ± 0.00 A Negative control 5.5 ± 0.17 B^(a)Damage ratings on individual plants were determined using thefollowing visual rating scale: 9. No visible leaf injury or a smallamount of pin or fine shot-hole type injury on a few leaves. 8. Smallamount of shot-hole type lesions on a few leaves. 7. Shot-hole injurycommon on several leaves. 6. Several leaves with shot-hole and elongatedlesions (Lesions <0.5″ in length). 5. Several leaves with elongatedlesions (Lesions 0.5″ to 1.0″ in length). 4. Several leaves withelongated lesions (Lesions >1.0″ in length). 3. Long lesions (>1.0″)common on about one-half the leaves. 2. Long lesions (>1.0″) common onabout two-thirds the leaves. 1. Most of the leaves with long lesions.^(b)Within a location, means with the same letter are not significantlydifferent (Fisher's Protected LSD test, P > 0.05).

For trials characterizing ECB2 damage, the same plants infested abovefor ECB1 were manually infested again later in the growing season withapproximately 100 ECB neonate larvae (300 larvae total) per plant 3times over approximately one week beginning at the R1 growth stage, whenapproximately 50% of the plants were shedding pollen. At approximately50-60 days after the last infestation, stalks of 8 consecutive plantsper plot (total of 24 plants per genetic background, per entry) weresplit from the top of the 4th internode above the primary ear to thebase of the plant. The total length of ECB stalk tunneling (ECBXCM) wasthen measured in centimeters and recorded for each plant. Tunnels 1 cmor less were considered entrance holes (larvae was not able to establishin the stalk) and were not included in the total cm of tunneling. Means(total cm of tunneling) were calculated for each treatment. The ECB2stalk feeding results for 4114 maize are shown in Table 10.

TABLE 10 Efficacy of DP-004114-3 Maize Against Second Generation ECBLarvae Mean ECBXCM (tunnel length, cm) ± Location Maize Line StandardError^(b) York, NE 4114 0.9 ± 0.27 B 1507 × 59122 0.4 ± 0.12 B Negativecontrol 22.6 ± 1.83 A  Mankato, MN 4114 1.3 ± 0.30 B 1507 × 59122 0.7 ±0.18 B Negative control 31.3 ± 2.19 A  Johnston, IA 4114 1.1 ± 0.26 B1507 × 59122 0.3 ± 0.11 B Negative control 33.0 ± 2.51 A  Princeton, IL4114 0.8 ± 0.22 B 1507 × 59122 0.1 ± 0.07 B Negative control 10.0 ± 0.94A  ^(b)Within a location, means with the same letter are notsignificantly different (Fisher's Protected LSD test, P > 0.05).

Root damage caused by WCRW was also investigated. Plants atapproximately the V2 growth stage were manually infested withapproximately 500 WCRW eggs applied into the soil on each side of theplant (˜1,000 eggs/plant total). Additionally, plots were planted infields that had a high probability of containing a natural infestationof WCRW. Plant roots were evaluated at approximately the R2 growthstage. Five consecutive plants per plot (total 45 plants per geneticbackground, per entry) were removed from the plot and washed withpressurized water. The root damage was rated using the 0-3 node injuryscale (CRWNIS) (Oleson, et al. (2005) J. Econ. Entomol. 98(1):1-8) andmeans were calculated for each treatment. Mean root damage ratings fromWCRW feeding are shown in Table 11.

TABLE 11 Efficacy of DP-004114-3 Maize Against WCR Larvae Mean CRWNISscore ± Location Maize Line Standard Error^(b,c) Johnston, IA 4114 0.1 ±0.01 B 1507 × 59122 0.1 ± 0.02 B Negative Control 0.5 ± 0.09 A Mankato,MN 4114 0.1 ± 0.02 B 1507 × 59122 0.1 ± 0.01 B Negative Control 1.1 ±0.11 A Rochelle, IL 4114 0.3 ± 0.04 B 1507 × 59122 0.1 ± 0.01 B NegativeControl 1.3 ± 0.18 A ^(b) Damage ratings on individual plant root masseswere determined using 0-3 Node Injury Scale (Oleson et al. 2005, supra).^(c) Within a location, means with the same letter are not significantlydifferent (Fisher's Protected LSD test, P > 0.05).

For the FAW efficacy testing, individual plants were manually infestedwith approximately 75 neonates at approximately the V5 growth stage.Leaves were scored for damage on 8 consecutive plants per plot (total of24 plants per genetic background, per entry) (FAWLF based on a 9-1visual rating scale where 9 indicates no damage and 1 indicates maximumdamage approximately two weeks after the last successful inoculation andmeans were calculated for each treatment. Mean damage ratingscharacterizing FAW foliar feeding on DP-004114-3 are shown in Table 12.

TABLE 12 Efficacy of DP-004114-3 Maize Against FAW Larvae Mean FAWLFDamage Rating ± Location Maize Line Standard Error^(a,b) Johnston, IA4114  8.9 ± 0.06 BC 1507 × 59122 9.0 ± 0.00 A Negative control 2.1 ±0.08 D ^(a)Damage ratings on individual plants were determined using thefollowing visual rating scale: 9. No damage to pinhole lesions presenton whorl leaves. 8. Pinholes and small circular lesions present on whorlleaves. 7. Small circular lesions and a few small elongated (rectangularshaped) lesions up to 0.5″ in length present on whorl and furl leaves.6. Several small elongated lesions 0.5″ to 1″ in length on a few whorland furl leaves. 5. Several large elongated lesions greater than 1″ inlength present on a few whorl and furl leaves and/or a few small tomid-sized uniform to irregular shaped holes (basement membrane consumed)in whorl and furl leaves. 4. Several large elongated lesions present onseveral whorl and furl leaves and/or several large uniform to irregularshaped holes in whorl and furl leaves. 3. Many elongated lesions of allsizes present on several whorl leaves plus several large uniform toirregular shaped holes in whorl and furl leaves. 2. Many elongatedlesions of all sizes present on most whorl and furl leaves plus many midto large-sized uniform to irregular shaped holes in whorl and furlleaves. 1. Whorl and furl leaves almost totally destroyed. ^(b)Within alocation, means with the same letter are not significantly different(Fisher's Protected LSD test, P > 0.05).

In addition to field efficacy studies, 4114 maize was evaluated in thelab-based sub-lethal seedling assay (SSA) (U.S. Publication No.2006/0104904 the contents of which is hereby incorporated by reference).The SSA allowed for a comparison of the efficacy of 4114 maize to anunprotected control (near isoline) without the confounding effects ofthe field environment. The SSA technique involves exposing a populationof neonate WCRW to maize seedlings containing either one of the 4114maize events or non-transgenic (negative control) maize seedlings.Larvae were exposed for a period of 17 days from the date of initial egghatch. The experimental unit for the SSA was a single plastic containerwith dimensions of 23×30×10 cm (Pactiv Corp., Lake Forest, Ill.).Entries were arranged in a randomized complete block with 3 replicationsper entry. For each entry, SSA setup involved placing 115 kernels intoeach container with 225 mL of a 1% thiophanate-methyl fungicide solutionand 1000 mL of Metro-Mix 200 plant growth media (Scotts-SierraHorticultural Products Company, Marysville, Ohio). Immediately afteradding the Metro-Mix, WCRW eggs were infested onto the surface of eachcontainer at a rate of 1,000 eggs per container. WCRW eggs werepre-incubated at 25° C. so that initial egg hatch was timed to occur 5-7days after container setup. Infested containers were held in a walk-inenvironmental chamber with settings of 25° C., 65% relative humidity,and 14:10 light:dark cycle. Larvae were extracted from the containers 17days post-egg hatch using a Burlese funnel system. A random subsample of30 larvae per container were selected and their head capsules measuredunder a dissecting microscope to categorize each into 1 of 3 instars.Data collected includes the age structure of the larval populationdetermined from the number of larvae in each of three potential instars.Histograms that graphically displayed the age distribution of larvae foreach entry were plotted and visually compared as shown in FIG. 4.

The pest spectrum for 4114 maize is provided in Table 13.

TABLE 13 Insect Pests That Are Controlled or Suppressed by DP-004114-3Maize Expressing Cry1F, Cry34Ab1, and Cry35Ab1 Scientific Name CommonName Insect Order Ostrinia nubilalis European corn borer (ECB)Lepidoptera Helicoverpa zea Corn earworm (CEW) Lepidoptera Spodopterafrugiperda Fall armyworm (FAW) Lepidoptera Diatraea grandiosellaSouthwestern corn borer Lepidoptera (SWCB) Richia albicosta Western beancutworm Lepidoptera (WBCW) Agrotis ipsilon Black cutworm (BCW)Lepidoptera Elasmopalpus lignosellus Lesser corn stalk borer (LCSB)Lepidoptera Diatrea crambidoides Southern corn stalk borer Lepidoptera(SCSB) Diabrotica virgifera Western corn rootworm Coleoptera virgifera(WCRW) Diabrotica virgifera zeae Mexican corn rootworm (MCR) ColeopteraDiabrotica berberi Northern corn rootworm (NCR) Coleoptera Diatreasaccharalis Sugarcane borer (SCB) Coleoptera

Example 6 Protein Expression and Concentration Generation of PlantMaterial

4114 maize from the PHNAR×BC3F3 generation was grown in five locationsin the United States and Canada. Each site employed a randomizedcomplete block design containing four blocks, with each block separatedby a buffer distance of at least 36 inches (0.9 m). Each entry wasplanted in 2-row plots bordered on each side by 1 row of border seed.

Leaf Tissue Collection and Processing

One leaf tissue sample was collected in each block at the V9 stage. Allsamples were collected from impartially selected, healthy,representative plants for each event. Each leaf sample was obtained byselecting the youngest leaf that had emerged at least 8 inches (20 cm,visible tissue) from the whorl. If this leaf was damaged or otherwiseunhealthy, the next leaf below it was sampled. The leaf was pruned (cut)from the plant approximately 8 inches (20 cm) from the leaf tip. Theleaf sample (including midrib) was cut into inch (2.5 cm) pieces andplaced in a 50-ml sample vial. The samples were then placed on dry iceuntil transferred to a freezer (≦−10° C.). Samples were shipped frozenand stored at ≦−10° C. upon arrival. All tissue samples werelyophilized, under vacuum, until dry. The lyophilized leaf samples werefinely homogenized in preparation for analysis. Samples were storedfrozen between processing steps.

Protein Concentration Determinations

Concentrations of the Cry1F, Cry34Ab1, Cry35Ab1, and PAT proteins weredetermined using specific quantitative ELISA methods.

Protein Extraction

Aliquots of processed leaf tissue samples were weighed into 1.2 mL tubesat the target weight of 10 mg. Each sample analyzed for Cry1F, Cry34Ab1,Cry35Ab1, and PAT protein concentrations was extracted in 0.6 mL ofchilled PBST (Phosphate Buffered Saline plus Tween-20). Followingcentrifugation, supernatants were removed, diluted, and analyzed.

Determination of Cry1F, Cry34Ab1 and PAT Protein Concentration

The Cry1F, Cry34Ab1 and PAT ELISA kits employed were obtained fromEnviroLogix, Inc. (Portland, Me.), and the Cry35Ab1 ELISA kit employedwas obtained from Acadia BioScience, LLC (Portland, Me.). The ELISAmethod for each of these four proteins utilized a sequential “sandwich”format to determine the concentration of the protein in sample extracts.Standards (analyzed in triplicate wells) and diluted sample extracts(analyzed in duplicate wells) were incubated in plate pre-coated with anantibody specific to a single protein chosen from Cry1F, Cry34Ab1,Cry35Ab1 or PAT. Following incubation, unbound substances were washedfrom the plate. A different specific antibody for the respectiveselected protein, conjugated to the enzyme horseradish peroxidase (HRP),was added to the plate and incubated. Then, unbound substances werewashed from the plate leaving the bound protein “sandwiched” between theantibody coated on the plate and the antibody-HRP conjugate. Detectionof the bound antibody-protein complex was accomplished by the additionof substrate, which generated a colored product in the presence of HRP.The reaction was stopped with an acid solution and the optical density(OD) of each well was determined using plate reader. An average of theresults from duplicate wells was used to determine the concentration ofthe Cry1F, Cry34Ab1, Cry35Ab1 or PAT protein in ng/mg sample dry weight.

Calculations for Determining Protein Concentrations

SoftMax® Pro software was used to perform the calculations required toconvert the OD values obtained by the plate reader to proteinconcentrations.

1. Standard Curve

A standard curve was included on each ELISA plate. The equation for thestandard curve was generated by the software, which used a quadratic fitto relate the mean OD values obtained for the standards to therespective standard concentration (ng/mL). The quadratic regressionequation was applied as follows:

y=Cx ² +Bx+A

where x=known standard concentration and y=respective mean absorbancevalue (OD).

2. Sample Concentration

Interpolation of the sample concentration (ng/ml) was accomplished bysolving for x in the above equation using values for A, B, and Cdetermined by the standard curve.

${{Sample}\mspace{14mu} {Concentration}\mspace{14mu} \left( {{ng}/{mL}} \right)} = \frac{{- B} + \sqrt{B^{2} - {4\; {C\left( {A - {sampleOD}} \right)}}}}{2\; C}$

e.g. Curve Parameters: A=0.0476, B=0.4556, C=−0.01910, and sampleOD=1.438

${{Sample}\mspace{14mu} {Concentration}} = {\frac{{- 0.4556} + \sqrt{0.4556^{2} - {4\left( {- 0.01910} \right)\left( {0.0476 - 1.438} \right)}}}{2\left( {- 0.01910} \right)} = {3.6\mspace{14mu} {{ng}/{mL}}}}$

Sample concentration values were adjusted for the dilution factorexpressed as 1:N

Adjusted Concentration=Sample Concentration×Dilution Factor

e.g. Sample Concentration=3.6 ng/mL and Dilution Factor=1:10

Adjusted Concentration=3.6 ng/mL×10=36 ng/mL

Adjusted sample concentration values were converted from ng/mL to ng/mgsample weight as follows:

ng/mg Sample Weight=ng/mL×Extraction Volume (mL)/Sample Weight (mg)

e.g. Concentration=36 ng/mL, Extraction Volume=0.60 ml, and

Sample Weight=10.0 mg

ng/mg Sample Weight=36 ng/mg×0.60 mL/10.0 mg=2.2 ng/mg

3. Lower Limit of Quantitation (LLOQ)

The LLOQ, in ng/mg sample weight, was calculated as follows:

${L\; L\; O\; Q} = \frac{{Reportable}\mspace{14mu} {Assay}\mspace{14mu} L\; L\; O\; Q \times {Extraction}\mspace{14mu} {Volume}}{{Sample}\mspace{14mu} {Target}\mspace{14mu} {Weight}}$

e.g. for PAT in leaf: reportable assay LLOQ=2.3 ng/mL, extractionvolume=0.6 mL, and sample target weight=10 mg

${L\; L\; O\; Q} = {\frac{2.3\mspace{14mu} {{ng}/{mL}} \times 0.6\mspace{14mu} {mL}}{10\mspace{14mu} {mg}} = {0.14\mspace{14mu} {{ng}/{mg}}\mspace{14mu} {sample}\mspace{14mu} {weight}}}$

Results

The proteins Cry1F, Cry34Ab1, Cry35Ab1, and PAT were detected in V9 leaftissue of 4114 maize at the concentrations set forth in Table 14 below.

TABLE 14 Protein Concentrations in 4114 Maize Protein concentration inng/mg dry weight* Cry1F Cry34Ab1 Cry35Ab1 PAT Mean ± SD 9.7 ± 2.5 26 ±3.1 33 ± 3.1 9.8 ± 3.3 Range 5.3-14 22-31 28-39 4.8-15 *The LLOQ forCry1F and PAT was 0.14 ng/mg Dry Weight; the LLOQ for Cry34Ab1 andCry35Ab1 were 0.16 ng/mg Dry Weight

Example 7 An Event-Specific Identification System for DP-004114-3 Maize

The event-specific system for DP-004114-3 maize was designed at the 5′junction between the DP-004114-3 insert and maize genomic region. Theforward primer (08-O-2677, SEQ ID NO: 29) is situated within maizegenomic DNA, the reverse primer (08-O-2678, SEQ ID NO: 30) is situatedwithin the inserted DNA, and the binding site of the probe (08-QP74, SEQID NO: 31) spans the transition between DP-004114-3 insert and maizegenomic DNA (Table 15). The optimum primer and probe concentrations wereselected based on PCR efficiency and the ability to quantitate at thelow (0.08% GM) and high (5% GM) ends of the dynamic range (Table 16).

TABLE 15 Primers and probe for DP-004114-3 event-specific PCR system SEQID Name Sequence  NO. 08-0-2677 5′-CGT TTG TAG CAC TTG CAC GTA GT-3′ 2908-0-2678 5′-GGT AAC CGC TCT TCC AGT TGA A-3′ 30 08-QP745′-AAG CTT CAA CAC AGA TC-3′ 31 (probe)DP-004114-3 amplicon sequence (underlined are the primer and probebinding sites): Length: 90 bp CGTTTGTAGCACTTGCACGTAGT TACCCGGACCGAAGCTTCAACACAGA TC TGATAGTTTAAACGCTC TTCAACTGGAAGAGCGGTTACC(SEQ ID NO: 32)

TABLE 16 Mastermix for DP-004114-3 event-specific PCR system FinalChemicals Concentration Concentration† μl/reaction Applied BiosystemsTaqMan 2× 1× 10.0 Universal PCR Master Mix, No AmpErase UNG 08-0-2677 10μM 500 nM 1.0 08-0-2678 10 μM 900 nM 1.8 08-QP74 10 μM 200 nM 0.4Sterile water 1.8 Total volume 15.0 †Total PCR reaction is 20 μl (15 μlmastermix and 5 μl genomic DNA template).

TABLE 17 Reaction and cycling parameters Format: 15 μl mastermix + 5 μlgenomic DNA template = 20 μl per reaction Equipment: Applied BiosystemsViiA7 real time thermal cycler Software: ViiA 7 RUO software version 1.1Plasticware: MicroAmp ® Optical 96-well Reaction Plates (AppliedBiosystems, Inc.); PRISM ™ 384-well Clear Optical Reaction Plates(Applied Biosystems, Inc.); and MicroAmp ™ Optical Adhesive Film(Applied Biosystems, Inc.)

TABLE 18 Cycling parameters Data Step Stage Temp. Time collection Cycles1 Initial enzyme activation 95° C. 600 s  no  1x 2 Amplification 95° C.15 s no 40x Denaturation 3 Annealing & Extension 60° C. 60 s Yes

The assay format used a standard curve having four standard points, eachin triplicate. The standards were produced by preparing a solution of 40ng/μl of total genomic maize DNA with 10% DP-004114-3 maize DNA followedby serial dilutions in 0.1×TE buffer containing 10 ng/μl salmon spermDNA. Negative controls (NTC) were measured in triplicate for each systemto verify purity of the reagents. Each sample (unknown) was analyzed at200 ng genomic maize DNA per reaction in triplicates (six reactions persample in total for both PCR systems). The relative content ofDP-004114-3 maize to total maize DNA was subsequently calculated bydetermining the mean of the copy numbers based on the standard curves(linear regression of threshold cycle (C_(T)) value versus log [copynumber]) and calculating the ratios of DP-004114-3 maize copynumber/total copy number of haploid maize genomes.

This event-specific quantitative PCR system for detection of DP-004114-3maize DNA was developed, optimized, and validated on Applied Biosystem'sViiA 7™ real-time PCR system. The method can also be applied on adifferent platform however, with minimal optimization and adaptation.

The event-specific real-time PCR method described here can be applied todetermine the relative content of DP-004114-3 maize DNA in total genomicmaize DNA. The method performs in a linear manner with an acceptablelevel of accuracy and precision over the whole range from 0.08% to 5.0%DP-004114-3 content. The method was developed and validated with genomicDNA extracted from maize seeds. However, the assay can be applied to anymatrix from which genomic DNA with sufficient quantity and quality canbe purified.

Example 8 Gel-Based PCR Detection Method for the Maize Event DP-004114-3

This protocol describes a qualitative gel-based PCR assay to detect thepresence of DP-004114-3 maize DNA. The PCR detection method is used inconjunction with a DNA extraction method which yields DNA of sufficientquality and quantity.

A PCR system for DP-004114-3 maize was developed using primers toamplify the 5′ border junction between maize genomic DNA and theDP-004114-3 insert. The forward primer is located in the maize genomicregion, and the reverse primer is located in the transgene insert.

Forward Primer (11-O-4127) (SEQ ID NO: 33):5′-GGA CCC TGT TCA CAA CAC AGG GCT C-3′Reverse Primer (11-O-4128) (SEQ ID NO: 34):5′-GGC CGA AGC TTC GGT CCG G-3′Amplicon Sequence (underlined are the primerbinding sites) (SEQ ID NO: 35):ggaccctgttcacaacacagggctctggctttggagcctctcgtttgtagcacttgcacgtagttacccggaccgaagcttcaacacagatctgatagtttaaacgctcttcaactggaagagcggttacccggaccgaagcttcggcc

Equipment and Materials Used:

Equipment/Plasticware Specification 96-well GeneAmp PCR System 9700Applied Biosystems, Foster City, Ca; or equivalent Gel ElectrophoresisUnit Sub Cell GT, Bio-Rad, Hercules, CA; or equivalent Power supplyPower Pac, Bio-Rad, Hercules, CA; or equivalent Gel documentationBio-Rad Molecular Imager Gel Doc XR+ Imager System; or equivalentQuantity One, 2.0 Software; or equivalent Pipettes with adjustablevolume Ranin, Woburn, MA; Research: 0.5-10 μl; 2-20 μl, 20-200 μl,100-1000 μl; or equivalent Filter Tips Appropriate for the pipettemodels used PCR Reaction tubes and Caps Applied Biosystems, Foster City,CA; or equivalent Reaction tubes 1.5 ml Eppendorf, Hamburg, Germany; orequivalent

Reagents, Buffers and Solutions:

Reagent Specification 2× Promega PCR Master Mix Promega, Madison, WI; orequivalent (contains 15 mM MgCl₂ and Taq polymerase) PCR Marker Promega,Madison, WI; or equivalent UltraPure Agarose Invitrogen, Carlsbad, CA;or equivalent Ethidium bromide EMD, Darmstadt, Germany; or equivalent 6×Promega Blue Orange Promega, Madison, WI; or equivalent Loading dye 10×TBE buffer Mediatech, Herndon, VA; or equivalent Molecular Grade WaterMediatech, Herndon, VA; or equivalent

Procedures

Reagents were thoroughly mixed before use. A reaction mix consisting ofall components of the PCR reaction were prepared, except template DNA,in sufficient quantity for all reactions to be performed. Reagents andthe master mix were kept on ice.

Preparation of the Mastermix for the PCR System:

Final Component Concentration Concentration μl/rxn Promega 2× PCR buffer2 x 1 x 12.50 Forward Primer (11-O-4127) 10 μM 200 nM 0.50 ReversePrimer (11-O-4128) 10 μM 200 nM 0.50 Sterile water 6.50 Total volume20.00

Components were mixed and 20 μl of the thoroughly mixed mastermixdispensed into reaction tubes. 5 μl of a 20 ng/μl template genomic DNAwere added.

No Template Controls: Instead of genomic DNA, 5 μl of the diluent usedfor diluting the test DNA samples were added to their properconcentration; e.g. water, 0.1×TE, etc.

Positive controls: 5 μl of e.g. 1% DP-004114-3 (20 ng/μl) maize DNA wereadded.

After addition of template to mastermix, reaction tubes were capped andimmediately placed in pre-heated PCR machine and run was initiated.

Cycling Parameters

The PCR assay was performed using an Applied Biosystems' 96-well GeneAmpPCR System 9700 with the ramp speed set to ‘GeneAmp 9600’. The cyclingparameters were as follows:

PCR Profile for DP-004114-3 Detection Method

Step Cycle element T (° C.) Time (min:sec) Cycles 1 Initial Denaturation95  2:00 1x 2 Amplification Denaturation 95 00:30 35x  3 Annealing 6600:30 4 Extension 72 00:30 5 Final Extension 72 07:00 1x

Gel Electrophoresis

PCR products were mixed with enough 6× loading buffer added for a finalconcentration of 1× loading buffer (example: 25 μl PCR product plus 5 μl6× loading buffer). 15 μl PCR products/loading dye mixture were loadedon a 2.5% agarose/1×TBE gel. Gel was run with a maximum of 7 V per cm(measured electrode to electrode) until the fragments were separatedproperly. Gel was run long enough to get clear separation of markerbands in the 50 to 200 bp range. The agarose gel was stained in anethidium bromide bath (1.5 μg per ml in distilled water or buffer) forapproximately 15 min, rinsed with distilled water or 1×TBE, andphotographed under UV-light with an appropriate gel-documentationsystem. The PCR product for DP-004114-3 maize was 149 bp in length.

Having illustrated and described the principles of the presentinvention, it should be apparent to persons skilled in the art that theinvention can be modified in arrangement and detail without departingfrom such principles. We claim all modifications that are within thespirit and scope of the appended claims.

All publications and published patent documents cited in thisspecification are incorporated herein by reference to the same extent asif each individual publication or patent application was specificallyand individually indicated to be incorporated by reference.

What is claimed is:
 1. An amplicon comprising the nucleic acid sequenceselected from the group consisting of SEQ ID NO: 32, SEQ ID NO: 35 andfull length complements thereof.
 2. A biological sample derived fromcorn event DP-004114-3 plant, tissue, or seed, wherein said samplecomprises a nucleotide sequence which is or is complementary to asequence selected from the group consisting of SEQ ID NO: 32 and SEQ IDNO: 35, wherein said nucleotide sequence is detectable in said sampleusing a nucleic acid amplification or nucleic acid hybridization method,wherein a representative sample of said corn event DP-004114-3 seed ofhas been deposited with American Type Culture Collection (ATCC) withAccession No. PTA-11506.
 3. The biological sample of claim 2, whereinsaid biological sample comprise plant, tissue, or seed of transgeniccorn event DP-004114-3.
 4. The biological sample of claim 3, whereinsaid biological sample is a DNA sample extracted from the transgeniccorn plant event DP-004114-3, and wherein said DNA sample comprises oneor more of the nucleotide sequences selected from the group consistingof SEQ ID NO: 32, SEQ ID NO: 35, and the complement thereof.
 5. Thebiological sample of claim 4, wherein said biological sample is selectedfrom the group consisting of corn flour, corn meal, corn syrup, cornoil, corn starch, and cereals manufactured in whole or in part tocontain corn by-products.
 6. An extract derived from corn eventDP-004114-3 plant, tissue, or seed and comprising a nucleotide sequencewhich is or is complementary to a sequence selected from the groupconsisting of SEQ ID NO: 32 and SEQ ID NO: 35, wherein a representativesample of said corn event DP-004114-3 seed has been deposited withAmerican Type Culture Collection (ATCC) with Accession No. PTA-11506. 7.The extract of claim 6, wherein said nucleotide sequence is detectablein said extract using a nucleic acid amplification or nucleic acidhybridization method.
 8. The extract of claim 7, wherein said extractcomprises plant, tissue, or seed of transgenic corn plant eventDP-004114-3.
 9. The extract of claim 8, further comprising a compositionselected from the group consisting of corn flour, corn meal, corn syrup,corn oil, corn starch, and cereals manufactured in whole or in part tocontain corn by-products, wherein said composition comprises adetectable amount of said nucleotide sequence.
 10. A method ofdetermining zygosity of DNA of a corn plant comprising corn eventDP-004114-3 in a biological sample comprising: (a) contacting saidsample with a primer pair selected from the group consisting of SEQ IDNOs: 29 and 30, or a primer pair selected from the group consisting ofSEQ ID NOs: 33 and 34, such that (1) when used in a nucleic acidamplification reaction comprising corn event DP-004114-3 DNA, produces afirst amplicon that is diagnostic for corn event DP-004114-3, and (2)when used in a nucleic acid amplification reaction comprising corngenomic DNA other than DP-004114-3 DNA, produces a second amplicon thatis diagnostic for corn genomic DNA other than DP-004114-3 DNA; (b)performing a nucleic acid amplification reaction; and (c) detecting theamplicons so produced, wherein detection of presence of both ampliconsindicates that said sample is heterozygous for corn event DP-004114-3DNA, wherein detection of only the first amplicon indicates that saidsample is homozygous for corn event DP-004114-3 DNA.
 11. A pair ofpolynucleotide primers comprising a first polynucleotide primer and asecond polynucleotide primer, wherein the first polynucleotide primercomprises the nucleotide sequence of SEQ ID NO: 29 and the complementthereof; and the second polynucleotide primer comprises the nucleotidesequence of SEQ ID NO: 30 and the complement thereof, which functiontogether in the presence of a DP-004114-3 DNA template in a sample toproduce an amplicon diagnostic for event DP-004114-3.
 12. A kit fordetecting nucleic acids that are unique to event DP-004114-3 comprisingis a primer pair consisting of SEQ ID NOs: 29 and 30, or SEQ ID NOs: 33and 34, and the complements thereof, which function as a primer pair ina nucleic acid detection method, and which upon amplification of orhybridization to a target nucleic acid sequence in a sample followed bydetection of the amplicon or hybridization to the target sequence, arediagnostic for the presence of nucleic acid sequences unique to eventDP-004114-3 in the sample.